EP2760836A1 - Aminsubstituierte methansulfonamidderivate als vanilloidrezeptorliganden - Google Patents

Aminsubstituierte methansulfonamidderivate als vanilloidrezeptorliganden

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Publication number
EP2760836A1
EP2760836A1 EP12762601.8A EP12762601A EP2760836A1 EP 2760836 A1 EP2760836 A1 EP 2760836A1 EP 12762601 A EP12762601 A EP 12762601A EP 2760836 A1 EP2760836 A1 EP 2760836A1
Authority
EP
European Patent Office
Prior art keywords
methyl
phenyl
pyridin
trifluoromethyl
propanamide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP12762601.8A
Other languages
English (en)
French (fr)
Inventor
Robert Frank-Foltyn
Gregor Bahrenberg
Thomas Christoph
Bernhard Lesch
Jeewoo Lee
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gruenenthal GmbH
Original Assignee
Gruenenthal GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gruenenthal GmbH filed Critical Gruenenthal GmbH
Priority to EP12762601.8A priority Critical patent/EP2760836A1/de
Publication of EP2760836A1 publication Critical patent/EP2760836A1/de
Withdrawn legal-status Critical Current

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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/10—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
    • C07D211/14—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with hydrocarbon or substituted hydrocarbon radicals attached to the ring nitrogen atom
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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Definitions

  • the invention relates to amine substituted methanesulfonamide derivatives as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
  • the subtype 1 vanilloid receptor (VR1/TRPV1 ), which is often also referred to as the capsaicin receptor, is a suitable starting point for the treatment of pain, in particular of pain selected from the group consisting of acute pain, chronic pain, neuropathic pain and visceral pain.
  • This receptor is stimulated inter alia by vanilloids such as capsaicin, heat and protons and plays a central role in the formation of pain.
  • the compounds should be suitable in particular as pharmacological active ingredients in pharmaceutical compositions, preferably in pharmaceutical compositions for the treatment and/or prophylaxis of disorders or diseases which are at least partially mediated by vanilloid receptors 1 (VR1/TRPV1 receptors).
  • VR1/TRPV1 receptors vanilloid receptors 1
  • substituted compounds of general formula (I), as given below display outstanding affinity to the subtype 1 vanilloid receptor (VR1 /TRPV1 receptor) and are therefore particularly suitable for the prophylaxis and/or treatment of disorders or diseases which are at least partially mediated by vanilloid receptors 1 (VR1 /TRPV1 ).
  • the present invention therefore relates to a substituted compound of general formula (I)
  • R 3 is selected from the group consisting of H, F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , 0-CF 3 , and NH 2 ,
  • Z represents N or C-R 4b , wherein R 4b represents H or CH 3 , R represents H or CH 3 ,
  • R 5 represents H or CH 3 , X represents N or CH;
  • R 6 represents CF 3 , an unsubstituted, saturated Ci -4 aliphatic residue or an unsubstituted, saturated C 3 - 6 cycloaliphatic residue,
  • R 7 represents H, or an unsubstituted Ci -4 aliphatic residue
  • R 8 represents a Ci -4 aliphatic residue, unsubstituted or mono-, di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, OH, 0-CH 3 , 0-CH 2 -OH, 0-CH 2 -0-CH 3 , 0-C 2 H 5 , 0-CH 2 -CH 2 -OH, 0-CH 2 - CH 2 -0-CH 3 , NH 2 , NH(CH 3 ), and N(CH 3 ) 2 , preferably an unsubstituted d_ 4 aliphatic residue; a C 3 -6 cycloaliphatic residue, optionally bridged via an unsubstituted, saturated Ci -4 aliphatic group, unsubstituted or mono-, or di-, or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I
  • R 7 and R 8 together with the nitrogen atom connecting them form a 3 to 6 membered heterocycloaliphatic residue, unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , C 2 H 5 , CH 2 -OH, CH 2 -CH 2 -OH, CH 2 -0-CH 3 , CH 2 -CH 2 -0-CH 3 , CH 2 - NH(CH 3 ), CH 2 -N(CH 3 ) 2 , CF 3 , OH, 0-CH 3 , 0-CH 2 -OH, 0-CH 2 -0-CH 3 , 0-C 2 H 5 , 0-CH 2 - CH 2 -OH, 0-CH 2 -CH 2 -0-CH 3 , 0-CF 3 , SH, S-CH 3 , S-CF 3 , NH 2 , NH(CH 3 ), N(
  • single stereoisomer comprises in the sense of this invention an individual enantiomer or diastereomer.
  • mixture of stereoisomers comprises in the sense of this invention the racemate and mixtures of enantiomers and/or diastereomers in any mixing ratio.
  • physiologically acceptable salt comprises in the sense of this invention a salt of at least one compound according to the present invention and at least one physiologically acceptable acid or base.
  • Ci -4 aliphatic residue comprises in the sense of this invention acyclic saturated or unsaturated aliphatic hydrocarbon residues, which can be branched or unbranched and also unsubstituted or mono- or polysubstituted if not indicated otherwise, which contain 1 to 4 carbon atoms (i.e. 1 , 2, 3 or 4 carbon atoms) respectively, i.e. Ci -4 alkanyls (Ci -4 alkyls), C 2 -4 alkenyls and C 2 -4 alkynyls, respectively.
  • aliphatic residues are selected from the group consisting of alkanyl (alkyl) and alkenyl residues, more preferably are alkanyl (alkyl) residues.
  • Preferred Ci -4 alkanyl residues are selected from the group consisting of methyl, ethyl, n-propyl, 2-propyl, n-butyl, isobutyl, sec- butyl, and tert.-butyl.
  • Preferred C 2 . 4 alkynyl residues are selected from the group consisting of ethynyl, propynyl (-CH 2 -C ⁇ CH, -C ⁇ C-CH 3 ) and butynyl.
  • C 3 . 6 cycloaliphatic residue means for the purposes of this invention cyclic aliphatic hydrocarbons containing 3, 4, 5 or 6 carbon atoms, wherein the hydrocarbons in each case can be saturated or unsaturated (but not aromatic), unsubstituted or mono- or polysubstituted, if not indicated otherwise.
  • the cycloaliphatic residues can be bound to the respective superordinate general structure via any desired and possible ring member of the cycloaliphatic residue.
  • the cycloaliphatic residues can also be condensed with further saturated, (partially) unsaturated, (hetero)cyclic, aromatic or heteroaromatic ring systems, i.e.
  • C 3 . 6 cycloaliphatic residues are selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclopentenyl, and cyclohexenyl.
  • Particularly preferred C 3 . 6 cycloaliphatic residues are C 5 - 6 cycloaliphatic residues such as cyclopentyl, cyclohexyl, cyclopentenyl and cyclohexenyl.
  • the heterocycloaliphatic residue can be bound to the superordinate general structure via any desired and possible ring member of the heterocycloaliphatic residue if not indicated otherwise.
  • the heterocycloaliphatic residues can also be condensed with further saturated, (partially) unsaturated (hetero)cycloaliphatic or aromatic or heteroaromatic ring systems, i.e. with cycloaliphatic, heterocycloaliphatic, aryl or heteroaryl residues, which can in turn be unsubstituted or mono- or polysubstituted, if not indicated otherwise.
  • heterocycloaliphatic residues which are condensed with a further ring system are e.g. indolinyl and isoindolinyl.
  • spirocycles i.e. an at least bicyclic ring system, wherein the 3-6-membered heterocycloaliphatic residue is connected through just one (spiro)atom with a further saturated, (partially) unsaturated (hetero)cycloaliphatic or aromatic or heteroaromatic ring system.
  • spirocycle is 1 -oxa-2,8-diazaspiro[4.5]dec-2-en-8-yl.
  • Preferred heterocycloaliphatic residues are selected from the group consisting of azetidinyl, aziridinyl, dithiolanyl, dihydropyrrolyl, dioxanyl, dioxolanyl, dihydropyridinyl, dihydrofuranyl, dihydroisoxazolyl, dihydrooxazolyl, imidazolidinyl, isoxazolidinyl, oxazolidinyl, morpholinyl, oxiranyl, oxetanyl, pyrrolidinyl, piperazinyl, 4-methylpiperazinyl, piperidinyl, pyrazolidinyl, pyranyl, tetrahydropyrrolyl, tetrahydropyranyl, in particular tetrahydro-2H-pyran-4-yl, tetrahydrofuranyl, tetrahydropyridinyl, tetrahydrothiophen
  • Preferred condensed heterocycloaliphatic residues are e.g. 1 -oxa-2,8- diazaspiro[4.5]dec-2-en-8-yl, dihydroquinolinyl, dihydroindenyl, dihydroisoquinolinyl, dihydroindolinyl, dihydroisoindolyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, tetrahydroindolinyl, tetrahydropyridoindolyl, tetrahydronaphthyl, and tetrahydrocarbolinyl.
  • aryl means for the purpose of this invention aromatic hydrocarbons having 6 to 14, i.e. 6, 7, 8, 9, 10, 1 1 , 12, 13 or 14 ring members, preferably having 6 to 10, i.e. 6, 7, 8, 9 or 10 ring members, including phenyls and naphthyls.
  • Each aryl residue can be unsubstituted or mono- or polysubstituted if not indicated otherwise, wherein the aryl substituents can be the same or different and in any desired and possible position of the aryl.
  • the aryl can be bound to the superordinate general structure via any desired and possible ring member of the aryl residue.
  • aryl residues can also be condensed with further saturated, (partially) unsaturated, (hetero)cycloaliphatic, aromatic or heteroaromatic ring systems, i.e. with a cycloaliphatic, heterocycloaliphatic, aryl or heteroaryl residue, which can in turn be unsubstituted or mono- or polysubstituted, if not indicated otherwise.
  • condensed aryl residues are benzodioxolanyl and benzodioxanyl.
  • aryl is selected from the group consisting of phenyl, 1 -naphthyl, 2-naphthyl, fluorenyl and anthracenyl, each of which can be respectively unsubstituted or mono- or polysubstituted.
  • a particularly preferred aryl is phenyl, unsubstituted or mono- or polysubstituted.
  • heteroaryl for the purpose of this invention represents a 5 or 6-membered cyclic aromatic residue containing at least 1 , if appropriate also 2, 3, 4 or 5 heteroatoms, wherein the heteroatoms are each selected independently of one another from the group S, N and O and the heteroaryl residue can be unsubstituted or mono- or polysubstituted, if not indicated otherwise; in the case of substitution on the heteroaryl, the substituents can be the same or different and be in any desired and possible position of the heteroaryl.
  • the binding to the superordinate general structure can be carried out via any desired and possible ring member of the heteroaryl residue if not indicated otherwise.
  • the heteroaryl can also be part of a bi- or polycyclic system having up to 14 ring members, wherein the ring system can be formed with further saturated, (partially) unsaturated, (hetero)cycloaliphatic or aromatic or heteroaromatic rings, i.e. with a cycloaliphatic, heterocycloaliphatic, aryl or heteroaryl residue, which can in turn be unsubstituted or mono- or polysubstituted, if not indicated otherwise.
  • heteroaryl residue is selected from the group consisting of benzofuranyl, benzoimidazolyl, benzothienyl, benzothiadiazolyl, benzothiazolyl, benzotriazolyl, benzooxazolyl, benzooxadiazolyl, quinazolinyl, quinoxalinyl, carbazolyl, quinolinyl, dibenzofuranyl, dibenzothienyl, furyl (furanyl), imidazolyl, imidazothiazolyl, indazolyl, indolizinyl, indolyl, isoquinolinyl, isoxazolyl, isothiazolyl, naphthyridinyl, oxazolyl, oxadiazolyl, phenazinyl, phenothiazinyl, phthalazinyl, pyrazolyl, pyridyl (2-pyridyl, 3-pyridyl
  • Ci -4 aliphatic group bridged via a Ci -4 aliphatic group with respect to residues as aryl, heteroaryl, a heterocycloaliphatic residue and a cycloaliphatic residue mean for the purpose of the invention that these residues have the above-defined meanings and that each of these residues is bound to the respective superordinate general structure via a Ci -4 aliphatic group.
  • the Ci-4 aliphatic group can in all cases be branched or unbranched, unsubstituted or mono- or polysubstituted, if not indicated otherwise.
  • the Ci -4 aliphatic group can in all cases be furthermore saturated or unsaturated, i.e.
  • the C -4 -aliphatic group is a Ci -4 alkylene group or a C 2 -4 alkenylene group, more preferably a Ci -4 alkylene group.
  • Ci -4 alkylene groups are selected from the group consisting of -CH 2 -, -CH 2 -CH 2 -, -CH(CH 3 )-, -CH 2 -CH 2 - CH 2 -, -CH(CH 3 )-CH 2 -, -CH(CH 2 CH 3 )-, -CH 2 -(CH 2 ) 2 -CH 2 -, -CH(CH 3 )-CH 2 -CH 2 -, -CH 2 - CH(CH 3 )-CH 2 -, -CH(CH 3 )-CH(CH 3 )-, -CH(CH 2 CH 3 )-CH 2 -, -C(CH 3 ) 2 -CH 2 -, -CH(CH 2 CH 2 CH 3 )- and -C(CH 3 )(CH 2 CH 3 )-.
  • Preferred C 2 - 4 alkynylene groups are selected from the group consisting of -C ⁇ C-, -C ⁇ C-CH 2 -, -C ⁇ C-CH 2 -CH 2 -, -C ⁇ C-CH(CH 3 )-, -CH 2 -C ⁇ C-CH 2 - and -C ⁇ C-C ⁇ C-.
  • substituted refers in the sense of this invention, with respect to the corresponding residues or groups, to the single substitution or multiple substitution (polysubstitution), e.g. disubstitution or trisubstitution, of one or more hydrogen atoms each independently of one another by at least one substituent.
  • polysubstitution e.g. disubstitution or trisubstitution
  • the multiple substitution can be carried out using the same or using different substituents.
  • substituted refers in the sense of this invention, with respect to the corresponding residues or groups, to the single substitution or multiple substitution (polysubstitution), e.g. disubstitution or trisubstitution, of one or more hydrogen atoms each independently of one another by at least one substituent.
  • polysubstitution e.g. disubstitution or trisubstitution
  • the multiple substitution can be carried out using the same or using different substituents.
  • a residue occurs multiply within a molecule, then this residue can have respectively different meanings for various substituents: if, for example, both R 7 and R 8 denote a Ci -4 aliphatic residue, then the Ci -4 aliphatic residue can e.g. represent methyl for R 7 and can represent ethyl for R 8 .
  • salt formed with a physiologically compatible acid or “salt of physiologically acceptable acids” refers in the sense of this invention to salts of the respective active ingredient with inorganic or organic acids which are physiologically compatible - in particular when used in human beings and/or other mammals.
  • physiologically acceptable acids are: hydrochloric acid, hydrobromic acid, sulphuric acid, methanesulphonic acid, p- toluenesulphonic acid, carbonic acid, formic acid, acetic acid, oxalic acid, succinic acid, tartaric acid, mandelic acid, fumaric acid, maleic acid, lactic acid, citric acid, glutamic acid, saccharic acid, monomethylsebacic acid, 5-oxoproline, hexane-1 -sulphonic acid, nicotinic acid, 2, 3 or 4-aminobenzoic acid, 2,4,6-trimethylbenzoic acid, oc-lipoic acid, acetyl glycine, hippuric acid, phosphoric acid, aspartic acid. Citric acid and hydrochloric acid are particularly preferred.
  • salt formed with a physiologically compatible base or “salt of physiologically acceptable bases” refers in the sense of this invention to salts of the respective compound according to the invention - as an anion, e.g. upon deprotonation of a suitable functional group - with at least one cation or base - preferably with at least one inorganic cation - which are physiologically acceptable - in particular when used in human beings and/or other mammals.
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , CF 3 , OH and 0-CH 3 .
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , CF 3 , OH and 0-CH 3 .
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , and 0-CH 3 . More preferably,
  • R 3 is selected from the group consisting of H, F, and CI, even more preferably denotes H or F, in particular H.
  • R a represents H
  • Z represents C-R 4b , wherein R 4b represents H or CH 3 , and R 4a represents H.
  • R 4a represents H, or
  • Z represents C-R 4b , wherein R 4b represents H, and R 4a represents H or CH 3 .
  • Z represents N and R 4a represents H;
  • Z represents CR 4b and R 4a and R 4b each represent H;
  • Z represents CR 4b and R 4a represents methyl and R 4b represents H;
  • Z represents CR 4b and R 4a represents H and R 4b represents methyl.
  • R 5 represents H.
  • X represents CH.
  • R 6 represents CF 3 , methyl, ethyl, 2-propyl, isobutyl, sec-butyl, tert.-butyl, cyclopropyl, cyclobutyl or cyclopentyl.
  • R 6 represents CF 3 , methyl, ethyl, 2-propyl, tert.-butyl, cyclopropyl, or cyclobutyl. More preferably,
  • R 6 represents CF 3 , tert.-Butyl or cyclopropyl.
  • R 7 represents H or an unsubstituted, saturated, Ci -4 aliphatic residue
  • R 8 represents a Ci -4 aliphatic residue, unsubstituted or mono- or disubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, OH, and 0-CH 3 ; a C 3 -6 cycloaliphatic residue, unsubstituted or mono-, or di-, or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , C 2 H 5 , CF 3 , OH, 0-CH 3 , NH 2 , NH(CH 3 ), and N(CH 3 ) 2 ; phenyl or pyridyl, in each case unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , C 2 H 5 , CF
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl or tert.-butyl,
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ;
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl or tert.-butyl,
  • FT represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclopentyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ; or together with the nitrogen atom connecting them form a 3 to 6 membered heterocycloaliphatic residue selected from the group consisting of azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl and morpholinyl, in each case independently of one another unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, or n-butyl,
  • FT represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted, preferably monoubstituted, with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, CH 3 , CF 3 , OH, and 0-CH 3 ; or together with the nitrogen atom connecting them form a 3 to 6 membered heterocycloaliphatic residue selected from the group consisting of azetidinyl, pyrrolidinyl, piperidinyl, piperazinyl and morpholinyl, in each case independently of one another unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consist
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl or tert.-butyl,
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclopentyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted, preferably monosubsituted, with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ; or
  • Y represents O, NR 13 or C(R 14 )(R 15 ),
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl or tert.-butyl,
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclopentyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ; or
  • T1 T1 ), wherein m denotes 0 or 1 , n denotes 0 or 1 , Y represents O, NR 13 or C(R 14 )(R 15 ),
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, or n-butyl,
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ; or
  • Y represents O, NR 13 or C(R
  • R 7 represents H, CH 3 , C 2 H 5 , or n-butyl
  • R represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or monosubstituted with F or CI, or
  • T1 (T1 ), wherein m denotes 0 or 1 , and n denotes 0 or 1 , and
  • Y represents C(R 14 )(R 15 ),
  • R 12 denotes H, or CH 3 .
  • R 13 denotes H, CH 3 , phenyl, or pyridyl, in each case unsubstituted.
  • a further particularly preferred embodiment of the compound of general formula (I) is an inventive compound corresponding to general formula (l-g),
  • R 8 represents H, CH 3 , or C 2 H 5
  • R 10 represents NH 2 , CH 3 , or C 2 H 5
  • the respective remaining residue of R 1 and R 2 is selected from the group consisting of H, F, CI, Br, I, CH 3 , CH 2 -OH, CH 2 -0-CH 3 , CF 3 , OH, and 0-CH 3 ,
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , and 0-CH 3 , Z represents N and
  • R represents H, or
  • Z represents C-R 4b , wherein R 4b represents H or CH 3 , and
  • R 4a represents H
  • R 5 represents H
  • X represents N or CH
  • R 6 represents CF 3 , tert.-Butyl or cyclopropyl
  • R 7 represents H, CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl or tert.-butyl,
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or mono-, or di- or trisubstituted with 1 , 2 or 3 substituents selected independently of one another from the group consisting of F, CI, Br, I, CH 3 , CF 3 , OH, 0-CH 3 , and 0-CF 3 ; or
  • R 8 represents H, CH 3 , or C 2 H 5
  • R 10 represents NH 2 , CH 3 , or C 2 H 5
  • the respective remaining residue of R 1 and R 2 is selected from the group consisting of H, F, CI, Br, I, CH 3 , CH 2 -OH, CH 2 -0-CH 3 , CF 3 , OH, and 0-CH 3 ,
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , and 0-CH 3 ,
  • R 4a represents H, or
  • Z represents C-R wherein R ,4b
  • R 5 represents H, X represents N or CH,
  • R 6 represents CF 3 , tert.-Butyl or cyclopropyl
  • R 7 represents H, CH 3 , C 2 H 5 , or n-butyl
  • R 8 represents CH 3 , C 2 H 5 , n-propyl, iso-propyl, n-butyl, tert.-butyl, cyclohexyl, or phenyl, wherein phenyl can be unsubstituted or monosubstituted with F or CI, or
  • T1 (T1 ), wherein m denotes 0 or 1 , and n denotes 0 or 1 , and
  • Y represents C(R 14 )(R 15 ),
  • R 12 denotes H, or CH 3 .
  • R 13 denotes H, CH 3 , phenyl, or pyridyl, in each case unsubstituted.
  • R 8 represents H, CH 3 , or C 2 H 5
  • R 10 represents NH 2 , CH 3 , or C 2 H 5
  • the respective remaining residue of R 1 and R 2 is selected from the group consisting of H, F, CI, Br, I, CH 3 , CH 2 -OH, CH 2 -0-CH 3 , CF 3 , OH, and 0-CH 3 ,
  • R 3 is selected from the group consisting of H, F, CI, CH 3 , and 0-CH 3 ,
  • R 4a represents H, or
  • Z represents C-R 4b , wherein R represents H or CH 3 , and R 4a represents H, R 5 represents H, X represents N or CH, R 6 represents CF 3 , tert.-Butyl or cyclopropyl, R 7 represents H, CH 3 , C 2 H 5 or C 4 H 9 , and
  • R 8 represents a saturated Ci -4 aliphatic residue, unsubstituted cyclohexyl, unsubstituted phenyl or phenyl monosubstituted with F or CI, or
  • R 7 and R 8 together represent -(CH 2 ) 3 - 5 -, -(CH 2 ) o -C(R 100 ) 2 -(CH 2 ) p -, -(CH 2 ) 2 -Q-(CH 2 ) 2 -, or -CH 2 - CH(CH 3 )-0-CH(CH 3 )-CH 2 -; wherein p represents 0, 1 or 2;
  • o 1 , 2 or 3;
  • Particularly preferred are compounds according to the invention from the group
  • a 50 per cent displacement of capsaicin which is present at a concentration of 100 nM
  • a FLIPR assay with CHO K1 cells which were transfected with the human VR1 gene at a concentration of less than 2,000 nM, preferably less than 1 ,000 nM, particularly preferably less than 300 nM, most particularly preferably less than 100 nM, even more preferably less than 75 nM, additionally preferably less than 50 nM, most preferably less than 10 nM.
  • the Ca 2+ influx is quantified in the FLIPR assay with the aid of a Ca 2+ - sensitive dye (type Fluo-4, Molecular Probes Europe BV, Leiden, the Netherlands) in a fluorescent imaging plate reader (FLIPR, Molecular Devices, Sunnyvale, USA), as described hereinafter.
  • a Ca 2+ - sensitive dye type Fluo-4, Molecular Probes Europe BV, Leiden, the Netherlands
  • FLIPR fluorescent imaging plate reader
  • substituted compounds according to the invention of the aforementioned general formula (I) and corresponding stereoisomers and also the respective corresponding acids, bases, salts and solvates are toxicologically safe and are therefore suitable as pharmaceutical active ingredients in pharmaceutical compositions.
  • the present invention therefore further relates to a pharmaceutical composition containing at least one compound according to the invention of the above- indicated formula (I), in each case if appropriate in the form of one of its pure stereoisomers, in particular enantiomers or diastereomers, its racemates or in the form of a mixture of stereoisomers, in particular the enantiomers and/or diastereomers, in any desired mixing ratio, or respectively in the form of a corresponding salt, or respectively in the form of a corresponding solvate, and also if appropriate optionally one or more pharmaceutically compatible auxiliaries.
  • a pharmaceutical composition containing at least one compound according to the invention of the above- indicated formula (I), in each case if appropriate in the form of one of its pure stereoisomers, in particular enantiomers or diastereomers, its racemates or in the form of a mixture of stereoisomers, in particular the enantiomers and/or diastereomers, in any desired mixing ratio, or respectively in the form of a
  • compositions according to the invention are suitable in particular for vanilloid receptor 1 -(VR1/TRPV1 ) regulation, preferably for vanilloid receptor 1 -(VR1/TRPV1 ) inhibition and/or for vanilloid receptor 1 -(VR1 /TRPV1 ) stimulation, i.e. they exert an agonistic or antagonistic effect.
  • the pharmaceutical compositions according to the invention are preferably suitable for the prophylaxis and/or treatment of disorders or diseases which are mediated, at least in part, by vanilloid receptors 1 .
  • the pharmaceutical composition according to the invention is suitable for administration to adults and children, including toddlers and babies.
  • the pharmaceutical composition according to the invention may be found as a liquid, semisolid or solid pharmaceutical form, for example in the form of injection solutions, drops, juices, syrups, sprays, suspensions, tablets, patches, capsules, plasters, suppositories, ointments, creams, lotions, gels, emulsions, aerosols or in multiparticulate form, for example in the form of pellets or granules, if appropriate pressed into tablets, decanted in capsules or suspended in a liquid, and also be administered as much.
  • the pharmaceutical composition according to the invention conventionally contains further physiologically compatible pharmaceutical auxiliaries which can for example be selected from the group consisting of excipients, fillers, solvents, diluents, surface-active substances, dyes, preservatives, blasting agents, slip additives, lubricants, aromas and binders.
  • physiologically compatible auxiliaries and also the amounts thereof to be used depend on whether the pharmaceutical composition is to be applied orally, subcutaneously, parenterally, intravenously, intraperitoneal ⁇ , intradermal ⁇ , intramuscularly, intranasally, buccally, rectally or locally, for example to infections of the skin, the mucous membranes and of the eyes.
  • Preparations in the form of tablets, dragees, capsules, granules, pellets, drops, juices and syrups are preferably suitable for oral application; solutions, suspensions, easily reconstitutable dry preparations and also sprays are preferably suitable for parenteral, topical and inhalative application.
  • the substituted compounds according to the invention used in the pharmaceutical composition according to the invention in a repository in dissolved form or in a plaster, agents promoting skin penetration being added if appropriate, are suitable percutaneous application preparations. Orally or percutaneously applicable preparation forms can release the respective substituted compound according to the invention also in a delayed manner.
  • the pharmaceutical compositions according to the invention are prepared with the aid of conventional means, devices, methods and process known in the art, such as are described for example in exceedingRemington's Pharmaceutical Sciences", A.R. Gennaro (Editor), 17 th edition, Mack Publishing Company, Easton, Pa, 1985, in particular in Part 8, Chapters 76 to 93. The corresponding description is introduced herewith by way of reference and forms part of the disclosure.
  • the amount to be administered to the patient of the respective substituted compounds according to the invention of the above-indicated general formula I may vary and is for example dependent on the patient's weight or age and also on the type of application, the indication and the severity of the disorder. Conventionally 0.001 to 100 mg/kg, preferably 0.05 to 75 mg/kg, particularly preferably 0.05 to 50 mg of at least one such compound according to the invention are applied per kg of the patient's body weight.
  • the pharmaceutical composition according to the invention is preferably suitable for the treatment and/or prophylaxis of one or more disorders and/or diseases selected from the group consisting of pain, preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, visceral pain and joint pain; hyperalgesia; allodynia; causalgia; migraine; depression; nervous affection; axonal injuries; neurodegenerative diseases, preferably selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease and Huntington's disease; cognitive dysfunctions, preferably cognitive deficiency states, particularly preferably memory disorders; epilepsy; respiratory diseases, preferably selected from the group consisting of asthma, bronchitis and pulmonary inflammation; coughs; urinary incontinence; overactive bladder (OAB); disorders and/or injuries of the gastrointestinal tract; duodenal ulcers; gastric ulcers; irritable bowel syndrome; strokes; eye irritations; skin irritations; neurotic skin diseases; allergic skin diseases; psoria
  • the pharmaceutical composition according to the invention is suitable for the treatment and/or prophylaxis of one or more disorders and/or diseases selected from the group consisting of pain, preferably of pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, visceral pain and joint pain; migraine; depression; neurodegenerative diseases, preferably selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease and Huntington's disease; cognitive dysfunctions, preferably cognitive deficiency states, particularly preferably memory disorders; inflammations, preferably inflammations of the intestine, the eyes, the bladder, the skin or the nasal mucous membrane; urinary incontinence; overactive bladder (OAB); medication dependency; misuse of medication; withdrawal symptoms in medication dependency; development of tolerance to medication, preferably development of tolerance to natural or synthetic opioids; drug dependency; misuse of drugs; withdrawal symptoms in drug dependency; alcohol dependency; misuse of alcohol and withdrawal symptoms in alcohol dependency.
  • pain preferably of pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, vis
  • the pharmaceutical composition according to the invention is suitable for the treatment and/or prophylaxis of pain, preferably of pain selected from the group consisting of acute pain, chronic pain, neuropathic pain and visceral pain.
  • the present invention further relates to a substituted compound according to general formula (I) and also if appropriate to a substituted compound according to general formula (I) and one or more pharmaceutically acceptable auxiliaries for use in vanilloid receptor 1 -(VR1 /TRPV1 ) regulation, preferably for use in vanilloid receptor 1 -(VR1 /TRPV1 ) inhibition and/or vanilloid receptor 1 -(VR1/TRPV1 ) stimulation.
  • the present invention therefore further relates to a substituted compound according to general formula (I) and also if appropriate to a substituted compound according to general formula (I) and one or more pharmaceutically acceptable auxiliaries for use in the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by vanilloid receptors 1 .
  • the present invention therefore further relates to a substituted compound according to general formula (I) and also if appropriate to a substituted compound according to general formula (I) and one or more pharmaceutically acceptable auxiliaries for use in the prophylaxis and/or treatment of disorders and/or diseases selected from the group consisting of pain, preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, visceral pain and joint pain; hyperalgesia; allodynia; causalgia; migraine; depression; nervous affection; axonal injuries; neurodegenerative diseases, preferably selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease and Huntington's disease; cognitive dysfunctions, preferably cognitive deficiency states, particularly preferably memory disorders; epilepsy; respiratory diseases, preferably selected from the group consisting of asthma, bronchitis and pulmonary inflammation; coughs; urinary incontinence; overactive bladder (OAB); disorders and/or injuries of the gastrointestinal tract; duodenal ulcers
  • a substituted compound according to general formula (I) and also if appropriate to a substituted compound according to general formula (I) and one or more pharmaceutically acceptable auxiliaries for use in the prophylaxis and/or treatment of pain, preferably of pain selected from the group consisting of acute pain, chronic pain, neuropathic pain and visceral pain.
  • the present invention further relates to the use of at least one compound according to general formula (I) and also if appropriate of one or more pharmaceutically acceptable auxiliaries for the preparation of a pharmaceutical composition for vanilloid receptor 1 - (VR1/TRPV1 ) regulation, preferably for vanilloid receptor 1 -(VR1/TRPV1 ) inhibition and/or for vanilloid receptor 1 -(VR1 /TRPV1 ) stimulation, and, further for the prophylaxis and/or treatment of disorders and/or diseases which are mediated, at least in part, by vanilloid receptors 1 , such as e.g.
  • disorders and/or diseases selected from the group consisting of pain preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, visceral pain and joint pain; hyperalgesia; allodynia; causalgia; migraine; depression; nervous affection; axonal injuries; neurodegenerative diseases, preferably selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease and Huntington's disease; cognitive dysfunctions, preferably cognitive deficiency states, particularly preferably memory disorders; epilepsy; respiratory diseases, preferably selected from the group consisting of asthma, bronchitis and pulmonary inflammation; coughs; urinary incontinence; overactive bladder (OAB); disorders and/or injuries of the gastrointestinal tract; duodenal ulcers; gastric ulcers; irritable bowel syndrome; strokes; eye irritations; skin irritations; neurotic skin diseases; allergic skin diseases; psoriasis; vitiligo; herpes simplex; inflammations, preferably inflammations of the intestine
  • Another aspect of the present invention is a method for vanilloid receptor 1 -(VR1/TRPV1 ) regulation, preferably for vanilloid receptor 1 -(VR1 /TRPV1 ) inhibition and/or for vanilloid receptor 1 -(VR1 /TRPV1 ) stimulation, and, further, a method of treatment and/or prophylaxis of disorders and/or diseases, which are mediated, at least in part, by vanilloid receptors 1 , in a mammal, preferably of disorders and/or diseases selected from the group consisting of pain, preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, visceral pain and joint pain; hyperalgesia; allodynia; causalgia; migraine; depression; nervous affection; axonal injuries; neurodegenerative diseases, preferably selected from the group consisting of multiple sclerosis, Alzheimer's disease, Parkinson's disease and Huntington's disease; cognitive dysfunctions, preferably cognitive deficiency states, particularly preferably memory
  • the effectiveness against pain can be shown, for example, in the Bennett or Chung model (Bennett, G.J. and Xie, Y.K., A peripheral mononeuropathy in rat that produces disorders of pain sensation like those seen in man, Pain 1988, 33(1 ), 87-107; Kim, S.H. and Chung, J.M., An experimental model for peripheral neuropathy produced by segmental spinal nerve ligation in the rat, Pain 1992, 50(3), 355-363), by tail flick experiments (e.g. according to D'Amour und Smith (J. Pharm. Exp. Ther. 72, 74 79 (1941 )) or by the formalin test (e.g. according to D. Dubuisson et al., Pain 1977, 4, 161 -174).
  • the present invention further relates to processes for preparing inventive compounds of the above- indicated general formula (I).
  • All reactions which can be applied for synthesizing the compounds according to the present invention can each be carried out under the conventional conditions with which the person skilled in the art is familiar, for example with regard to pressure or the order in which the components are added. If appropriate, the person skilled in the art can determine the optimum procedure under the respective conditions by carrying out simple preliminary tests.
  • the intermediate and end products obtained using the reactions described hereinbefore can each be purified and/or isolated, if desired and/or required, using conventional methods known to the person skilled in the art. Suitable purifying processes are for example extraction processes and chromatographic processes such as column chromatography or preparative chromatography.
  • All of the process steps of the reaction sequences which can be applied for synthesizing the compounds according to the present invention as well as the respective purification and/or isolation of intermediate or end products, can be carried out partly or completely under an inert gas atmosphere, preferably under a nitrogen atmosphere.
  • substituted compounds according to the invention can be isolated both in the form of their free bases, their free acids and also in the form of corresponding salts, in particular physiologically compatible salts, i.e. physiologically acceptable salts.
  • the free bases of the respective substituted compounds according to the invention can be converted into the corresponding salts, preferably physiologically compatible salts, for example by reaction with an inorganic or organic acid, preferably with hydrochloric acid, hydrobromic acid, sulphuric acid, methanesulphonic acid, p-toluenesulphonic acid, carbonic acid, formic acid, acetic acid, oxalic acid, succinic acid, tartaric acid, mandelic acid, fumaric acid, maleic acid, lactic acid, citric acid, glutamic acid, saccharic acid, monomethylsebacic acid, 5-oxoproline, hexane-1 -sulphonic acid, nicotinic acid, 2, 3 or 4-aminobenzoic acid, 2,4,6-trimethylbenzoic acid, oc-lipoic acid, acetyl glycine, hippuric acid, phosphoric acid and/or aspartic acid.
  • an inorganic or organic acid preferably
  • the free bases of the respective substituted compounds of the aforementioned general formula (I) and of corresponding stereoisomers can likewise be converted into the corresponding physiologically compatible salts using the free acid or a salt of a sugar additive, such as for example saccharin, cyclamate or acesulphame.
  • a sugar additive such as for example saccharin, cyclamate or acesulphame.
  • the free acids of the substituted compounds according to the invention can be converted into the corresponding physiologically compatible salts by reaction with a suitable base.
  • substituted compounds according to the invention and of corresponding stereoisomers can if appropriate, like the corresponding acids, the corresponding bases or salts of these compounds, also be obtained in the form of their solvates, preferably in the form of their hydrates, using conventional methods known to the person skilled in the art.
  • substituted compounds according to the invention are obtained, after preparation thereof, in the form of a mixture of their stereoisomers, preferably in the form of their racemates or other mixtures of their various enantiomers and/or diastereomers, they can be separated and if appropriate isolated using conventional processes known to the person skilled in the art. Examples include chromatographic separating processes, in particular liquid chromatography processes under normal pressure or under elevated pressure, preferably MPLC and HPLC processes, and also fractional crystallisation processes.
  • the stationary phase used for the column chromatography was silica gel 60 (0.04 - 0.063 mm) from E. Merck, Darmstadt.
  • the mixing ratios of solvents or eluents for chromatography are specified in v/v.
  • the exemplary compounds 1 -6, 8-9, 14, 17, 21 , 24-25, 28-30, 34-35, 45-61 and 63-66 were obtained by one of the methods disclosed before or thereafter.
  • the exemplary compounds 7, 10-13, 15-16, 18-20, 22-23, 26-27, 31 -33, 36-44, 62 as well as 67-72 can be obtained by one of the methods disclosed before or thereafter.
  • the person skilled in the art is aware which method has to be employed to obtain a particular exemplary compound.
  • Step 1 To the solution of 2-(3-cyanophenyl)acetic acid (700 mg, 43.4 mmol ) in methanol was slowly added sulfuric acid (0.42 ml_, 4.34 mmol) at room temperature. The reaction mixture was refluxed for 3 h at 70 ° C under nitrogen atmosphere. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. Solvent was removed in vacuo and extracted with ethyl acetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column
  • Step 2 To the cooled solution of sodium hydride (91 mg, 2.285 mmol, 60 % suspension in oil) in anhydrous tetrahydrofuran was added a solution of methyl 2-(3-cyanophenyl)acetate (400 mg, 2.285 mmol) drop wise at 0 ° C. Reaction mixture was stirred at room temperature for 1 h. TLC showed complete consumption of starting material. The reaction mixture was quenched with brine and extracted with ethyl acetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column chromatography to afford methyl 2-(3-cyanophenyl)propanoate (180 mg, 48 %).
  • Step 3 A solution of methyl 2-(3-cyanophenyl)propanoate (180 mg, 9 mmol) in water and tetrahydrofuran (1 :2, 30 mL) was treated with lithium hydroxide (27 mmol) at 0 °C and stirred for 2 h at room temperature. The mixture was diluted with water and dichloromethane, acidified with 1 N HCI solution and extracted with dichloromethane several times. The combined organic layers were washed with water and brine, dried over magnesium sulfate and concentrated in vacuo which offered 2-(3-cyanophenyl)propanoic acid (147 mg, 88 %).
  • Step 4 A solution of 2-(3-cyanophenyl)propanoic acid (7 4mg, 42.2 mmol) in 1 ,4-dioxane was cooled in an ice bath and N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (120 mg, 63.2 mmol), 1 -hydroxybenzotriazole (85 mg, 63.2 mmol), triethylamine (127 ⁇ _, 126 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (1 15 mg, 42.2 mmol) were added consecutively. The reaction mixture was stirred overnight at room temperature.
  • Step 5 To a stirred solution of 2-(3-cyanophenyl)-N-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (100 mg, 23.2 mmol) in dry ethanol (15 mL), cooled to 0 °C were added nickel(ll) chloride hexahydride (55 mg, 23.2 mmol). Sodium borohydride (52 mg, 139 mmol) was added in small portions over 10 min. The reaction mixture was allowed to warm to room temperature and stirred for a further 1 h. The purple residue was dissolved in ethyl acetate (50 mL) and extracted with saturated NaHC0 3 .
  • Step 1 To the solution 2-(3-cyanophenyl)acetic acid (700 mg, 43.4 mmol ) in methanol was slowly added sulfuric acid (0.42 ml_,4.34 mmol, 0.1 eq) at room temperature. The reaction mixture was refluxed for 3 h at 70 °C under N 2. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. Solvent was removed in vacuo and extracted with ethylacetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column chromatography to afford methyl 2-(3-cyanophenyl)acetate (660 mg, 84 %)
  • Step 2 To the cooled solution of sodium hydride (91 mg, 2.285 mmol, 60 % suspension in oil) in anhydrous tetrahydrofuran was added solution of methyl 2-(3-cyanophenyl)acetate (400 mg, 2.285 mmol) dropwise at 0 °C. Reaction mixture was stirred at room temperature for 1 h.TLC showed complete consumption of starting material. The reaction mixture was quenched with brine and extracted with ethylacetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column chromatography to afford methyl 2-(3-cyanophenyl)propanoate (180 mg, 48 %)
  • Step 3 A solution of methyl 2-(3-cyanophenyl)propanoate (180 mg, 9 mmol) in water and tetrahydrofuran (1 :2, 30 ml_) was treated with lithium hydroxide (27 mmol) at 0° C and stirred for 2 h at room temperature. The mixture was diluted with water and dichloromethane, acidified with 1 N HCI solution, and extracted with dichloromethane several times. The combined organic layers were washed with water and brine, dried over magnesium sulfate, and concentrated in vacuo which offered 2-(3-cyanophenyl)propanoic acid (147 mg, 88 %)
  • Step 4 A solution of the 2-(3-cyanophenyl)propanoic acid (99 mg, 0.52 mmol) in dioxane was cooled in an ice bath and N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (148 mg, 0.78 mmol), 1 -hydroxybenzotriazole (108 mg, 0.78 mmol), triethylamine (167 ⁇ , 1 .57mmol) and the (2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (137 mg, 0.52 mmol), were added consecutively. The reaction mixture was stirred overnight at room temperature.
  • Step 5 To a stirred solution of 2-(3-cyanophenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (95 mg, 0.236 mmol) in dry ethanol (15 ml_), cooled to 0 °C, were added NiCI 2 -6 H 2 0 (56 mg, 0.236 mmol). Sodium borohydride (62 mg, 1 .65 mmol) was then added in small portions over 10 min. The reaction was exothermic and effervescent.
  • Step 6 A cooled solution of 2-(3-(aminomethyl)phenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (75 mg, 0.18 mmol) in dichloromethane was added triethylamine (22 ⁇ _, 0.22 mmol) at 0 °C resulting solution was treated dropwise with methanesulfonyl chloride (25.4 ⁇ , 0.221 mmol) over 10 min and stirred for 1 h at room temperature. After aqueous workup, the residue was purified by flash column
  • Step 1 To a solution of 2-(4-bromophenyl)acetic acid (3 g, 13.95 mmol) in ethanol was slowly added sulfuric acid (0.3 ml_, cat.) at room temperature. The reaction mixture was heated to 100 °C for overnight. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature and neutralized with NaHC0 3 . The mixture was extracted with ethyl acetateand washed with water and brine. The extract was dried over magnesium sulfate and concentrated under reduced pressure to give ethyl 2-(4- bromophenyl)acetate (3.24 g, 96 %).
  • Step 2 To a solution of ethyl 2-(4-bromophenyl)acetate ( 3.24 g, 13.32 mmol) in anhydrous dimethylformamide was added zinc cyanide (939 mg, 7.99 mmol) ,
  • Step 3 To a solution of ethyl 2-(4-(iminomethyl)phenyl)acetate (962 mg, 5.08 mmol) in anhydrous dimethylformamide was slowly added sodium hydride (224 g, 5.59 mmol) and iodomethane (0.33 ml_, 5.34 mmol) at 0°C. The reaction mixture was heated to room temperature for 45 min under N 2 . TLC showed complete consumption of starting material. The reaction mixture was added water for quenching. The mixture was extracted with ethyl acetate and washed with water and brine. The extract was dried over magnesium sulfate and concentrated under reduced pressure to afford crude which was purified by column chromatography to afford ethyl 2-(4-cyanophenyl)propanoate (832 mg, 81 %)
  • Step 4 To a stirred solution of ethyl 2-(4-cyanophenyl)propanoate (832 mg, 4.09 mmol) in co-solvent with tetrahydrofuran and water (1 :1 ) were added sodium hydroxide (409 mg, 10.23 mmol). The reaction mixture was stirred for overnight at room temperature, then acidified to pH 3-4 with acetic acid. The residue was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude 2-(4-cyanophenyl)propanoic acid (805 g) was obtained as 95 % yield.
  • Step 5 To a stirred solution of 2-(4-cyanophenyl)propanoic acid (50 mg, 0.29 mmol) in acetonitrile were added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (82 mg, 0.43 mmol), 1 -hydroxybenzotriazole (58 mg, 0.43 mmol), (2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3- yl)methanamine (77 mg, 0.31 mmol) and triethylamine (0.10 ml_, 0.71 mmol). The reaction mixture was stirred for overnight at room temperature.
  • Step 6 To a stirred solution of 2-(4-cyanophenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (56 mg, 0.14 mmol) in ethanol was cooled to 0 ° C and added NiCI 2 -6 H 2 0 (33 mg, 0.14 mmol) and stirred more than 15 min. Sodium borohydride (37 mg, 0.97 mmol) was then added in small portions. The reaction was exothermic and effervescent. The resulting reaction mixture was allowed to warm to room temperature and left to stir for 2 h. The mixture was filtered using celite pad. The filtrate was concentrated was evaporated.
  • Step 7 To a stirred solution of 2-(4-(aminomethyl)phenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (58 mg, 0.14 mmol) in pyridine was added methanesulfonylchloride (0.014 ml_, 0.19 mmol) The reaction mixture was stirred for overnight at room temperature. The mixture was diluted with ethyl acetate and washed with 1 N HCI and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Step 1 To a solution of (4-nitrophenyl)methanol (2 g, 13.06 mmol) in toluene (10 mL) was slowly added methane sulfonylchloride (1 .21 mL, 15.67 mmol) at room temperature. The reaction mixture was heated to 80 ° C for 4 h. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. The mixture was extracted with ethyl acetate and washed with water and brine. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give 4-nitrobenzyl methanesulfonate (2.2 g, 72 %).
  • Step 2 A solution of 4-nitrobenzyl methanesulfonate (2.2 g, 9.51 mmol) in
  • Step 3 2-(4-Nitrobenzyl)isoindoline-1 ,3-dione (1 .4 g, 4.96 mmol) was dissolved in
  • Step 4 (4-Nitrophenyl)methanamine (651 mg, 4.28 mmol) was dissolved in pyridine (4 ml_). The reaction mixture was added methane sulfonyl chloride (0.43 ml_, 5.56 mmol) and stirred for 1 h at room temperature. TLC showed complete consumption of starting material. The mixture was diluted with 1 N HCI and extracted with ethyl acetate. The extract was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give N-(4-nitrobenzyl)methanesulfonamide (881 mg, 89 %).
  • Step 5 N-(4-Nitrobenzyl)methanesulfonamide (881 mg, 3.83 mmol) was dissolved in methanol/tetrahydrofuran (1 :1 , 35 ml_). 10 % Pd / C (264 mg, 3 eq) was added to it. The resulting mixture was stirred at room temperature for overnight under H 2 . TLC showed complete consumption of starting material. The mixture was filtered through celite bed and the filterate was concentrated under reduced pressure. The crude was purified by column chromatography to give N-(4-aminobenzyl)methanesulfonamide (352 mg, 46 %).
  • Step 6 N-(4-Aminobenzyl)methanesulfonamide (352 mg, 1 .76 mmol) was dissolved in acetonitrile (3 mL) and tetrahydrofuran (4 mL). The reaction mixture was added pyridine (0.17 mL, 2.1 1 mmol) and phenyl chloroformate (0.23 mL, 1 .85 mmol) and stirred at room temperature for 3 h under nitrogen atmosphere. TLC showed complete consumption of starting material. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic part was washed with water and brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The crude was purified by column chromatography to give phenyl 4-(methylsulfonamidomethyl)phenylcarbamate (438 mg, 78 %).
  • Step 7 To a solution of phenyl 4-(methylsulfonamidomethyl)phenylcarbamate (57 mg, 0.18 mmol) in acetonitrile (3 mL) was added 4-dimethylaminopyridine ( 22 mg, 0.18 mmol) and (2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (44 mg, 0.18 mmol) at room temperature. The reaction mixture was stirred at 50 ° C for overnight. TLC showed complete consumption of starting material. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic part was washed with water and brine.
  • Step 1 To a stirred solution of (4-nitrophenyl)methanol (299 mg, 1 .952 mmol) in
  • Step 2 To a stirred solution of 4-nitrobenzyl methanesulfonate (333 mg, 1 .440 mmol) in dimethylformamide were added potassium phthalimide (293 mg, 1 .584 mmol). The reaction mixture was stirred for 16 h. The mixture was dissolved in ethyl acetate, washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(4- Nitrobenzyl)isoindoline-1 ,3-dione (535 mg) was obtained as crude.
  • Step 3 To a stirred solution of 2-(4-nitrobenzyl)isoindoline-1 ,3-dione (218 mg, 0.772 mmol) in tetrahydrofuran were added hydrazine monohydrate (246 mg, 3.089 mmol) and p- toluenesulfonic acid monohydrate (15 mg, 0.0772 mmol). The reaction mixture was stirred for 4 h at 80 ° C, then cooled to room temperature and diluted with ethyl acetate. The mixture was washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. (4-Nitrophenyl)methanamine (46 mg, 39 %) was obtained.
  • Step 4 To a stirred solution of (4-nitrophenyl)methanamine (46 mg, 0.302 mmol) in pyridine, cooled to 0 ° C, were added methanesulfonyl chloride (46 mg). The resulting reaction mixture was stirred for 1 h at room temperature. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(4- Nitrobenzyl)methanesulfonamide (43 mg, 62 %) was obtained.
  • Step 5 To a stirred solution of N-(4-nitrobenzyl)methanesulfonamide (43 mg, 0.188 mmol) in ethyl acetate were added 10 % Pd / C (5 mg). The mixture was charged with hydrogen gas balloon. The resulting mixture was stirred for 3 h, then filtered using celite. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(4- Aminobenzyl)methanesulfonamide (41 mg, 99 %) was obtained.
  • Step 6 To a stirred solution of N-(4-aminobenzyl)methanesulfonamide (41 mg, 0.204 mmol) in tetrahydrofuran and acetonitrile as co-solvent were added phenylchloroformate (34 mg, 0.2142 mmol) and pyridine (0.02 ml_, 0.2448 mmol). The reaction mixture was stirred for 3 h at room temperature. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. Phenyl 4- (methylsulfonamidomethyl)phenylcarbamate (54 mg, 83 %) was obtained.
  • Step 7 To a stirred solution of phenyl 4-(methylsulfonamidomethyl)phenylcarbamate (26 mg, 0.081 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (22 mg, 0.081 mmol) in acetonitrile were added 4-dimethylaminopyridine (10 mg, 0.081 mmol). The reaction mixture was stirred for 15 h at 50 ° C. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo.
  • Step 1 (4-Bromophenyl)methanamine (500 mg, 2.687 mmol) was dissolved in pyridine (5 ml_) and methanesulfonyl chloride (0.4 ml_, 5.106 mmol) was added to the solution at 0 ° C. The mixture was stirred for 1 h at 0 ° C. Then, the mixture was quenched with 1 N HCI solution and extracted with ethyl acetate.
  • Step 2 To a solution of N-(4-bromobenzyl)methanesulfonamide (663 mg, 2.51 mmol) in dimethylformamide, Manganese (276 mg, 5.02 mmol), NiBr 2 (bipy) (66 mg, 0.176 mmol), ethyl 2-chloropropanoate (0.42 ml_, 3.263 mmol) and trifluoroacetic acid (0.005 ml_, 0.065 mmol) were added. The reaction mixture was stirred for 60 h at 65 °C, quenched by concentrated HCI solution, extracted with diethyl ether, dried over magnesium sulfate and concentrated under reduced pressure.
  • Step 3 To a solution of ethyl 2-(4-(methylsulfonamidomethyl)phenyl)propanoate (413 mg) in tetrahydrofuran - water mixture, sodium hydroxide (145 mg) was added at room temperature. The mixture was stirred for overnight, extracted with ethyl acetate, dried over magnesium sulfate. The solvent was evaporated by vacuo, the residue purified by column
  • Step 4 2-(4-(Methylsulfonamidomethyl)phenyl)propanoic acid (55 mg , 0.214 mmol) and (2- (4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (64 mg, 0.235 mmol) were dissolved in 1 ,4-dioxane.
  • Step 1 To a stirred solution of (4-bromo-2-fluorophenyl)methanamine (2.5 g, 12.25 mmol) in pyridine (10 mL) at 0 °C in a protective gas atmosphere was added methanesulfonyl chloride (1 .422 mL, 18.38 mmol) slowly in portions. After addition, the suspension was stirred at 0 ° C for 1 h. The reaction mixture was diluted with ice cold water (20 mL) and pH was adjusted to ⁇ 1 using 16 % aqueous HCI solution. The resulting precipitation was filtered off, washed with ethyl acetate (3 x 20 mL) and dried overnight. The crude N-(4-bromo-2-fluorobenzyl)- methanesulfonamide (3.14 g, 91 %) was used as such without further purification.
  • Step 2 N-(4-bromo-2-fluorobenzyl)methanesulfonamide (2 g, 7.09 mmol) and ethyl-2- chloropropionate (1 .174 mL, 9.21 mmol) were dissolved in dimethylformamide (1 1 mL) in a protective gas atmosphere at room temperature. Subsequently, manganese (779 mg, 14.178 mmol), (2,2'-bipyridine)nickel(ll) dibromide (186 mg, 0.496 mmol) and trifluoroacetic acid (0.014 mL) were added and the mixture was stirred at 65 °C for 36 h.
  • reaction mixture was cooled to room temperature, hydrolysed using 1 N HCI (25 mL) and extracted with diethyl ether (4 x 25 mL). The combined organic layer were washed with water (25 mL) and brine (25 mL) and dried over magnesium sulfate. The solvent was evaporated under reduced pressure and the obtained residue was purified by column chromatography (silica gel: 100- 200 mesh, eluent: diethyl ether / n-hexane 10:1 ) to afford ethyl 2-(3-fluoro-4- (methylsulfonamidomethyl)phenyl)propanoate (342 mg, 16 %).
  • Step 4 To a stirred solution of 2-chloro-6-(trifluoromethyl)nicotinonitrile (1 g, 4.85 mmol) in tetrahydrofuran (10 mL) was added ethanamine (0.78 g, 12.12 mmol) and stirred for 12 h at room temperature. The reaction mixture was diluted with 1 N HCI (10 mL) and extracted with ethyl acetate (2 x 25 mL). The combined organic layer was washed with 1 N HCI (15 mL) and brine, dried over magnesium sulfate and concentrated under reduced pressure to afford 2- (ethylamino)-6-(trifluoromethyl)nicotinonitrile (1 .01 g, 97 %).
  • Step 5 2-(Ethylamino)-6-(trifluoromethyl)nicotinonitrile (1 g, 4.647 mmol) was dissolved in 2M methanolic ammonia solution (182 mL, 0.025 mmol/mL) and hydrogenated in a H-cube apparatus (flow rate 1 mL/min, 80 °C, 10 bar). The solvent was evaporated under reduced pressure to afford 3-(aminomethyl)-N-ethyl-6-(trifluoromethyl)pyridin-2-amine (948 mg, 93 %) as pure compound.
  • Step 6 To a stirred solution of 3-(aminomethyl)-N-ethyl-6-(trifluoromethyl)pyridin-2-amine (57 mg, 0.263 mmol) and 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoic acid (72 mg, 0.263 mmol) in tetrahydrofuran (2 mL) were added 1 -hydroxybenzotriazol (0.036 mL, 0.263 mmol), 0-(1 H-benzotriazol-1 -yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (85 mg, 0.263 mmol) and N-ethyldiisopropylamine (0.134 mL, 0.789 mmol).
  • reaction mixture was stirred for 42 h at room temperature.
  • the reaction mixture was concentrated under reduced pressure and the solid obtained was purified by column chromatography (silica gel: 100-200 mesh, eluent: ethyl acetate / cyclohexane 3:2) to afford N-((2-(ethylamino)-6- (trifluoromethyl)pyridin-3-yl)methyl)-2-(3-fluoro-4-(methylsulfonamido- methyl)phenyl)propanamide (example 8) (69 mg, 55 %).
  • Step 1 To a stirred solution of 2-fluoro-1 -methyl-4-nitrobenzene (1 .993 g, 12.85 mmol) in carbon tetrachloride were added benzoyl peroxide (497 mg, 1 .2847 mmol) and N- bromosuccinimide (2.972 g, 16.701 mmol). The reaction mixture was refluxed for 18 h, then cooled to room temperature. The mixture was dissolved in ethyl acetate, then washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography to gave 1 - (bromomethyl)-2-fluoro-4-nitrobenzene (780 mg, 26 %).
  • Step 2 To a stirred solution of 1 -(bromomethyl)-2-fluoro-4-nitrobenzene (780 mg, 3.3 mmol) in dimethylformamide were added potassium phthalimide (1 .235 g, 6.67 mmol). The reaction mixture was stirred for 18 h at room temperature. The mixture was dissolved in ethyl acetate, washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2- (2-Fluoro-4-nitrobenzyl)isoindoline-1 ,3-dione (1 .034 g) was obtained as crude.
  • Step 3 To a stirred solution of 2-(2-fluoro-4-nitrobenzyl)isoindoline-1 ,3-dione (1 .034 g, 3.44 mmol) in tetrahydrofuran were added hydrazine monohydrate (1 .104 g, 13.77 mmol) and p- toluenesulfonic acid monohydrate (66 mg, 0.34 mmol). The reaction mixture was refluxed for 6 h, then cooled to room temperature and diluted ethyl acetate. The mixture was washed with water and brine. The organic layer was dried over magnesium sulfate and the solvent removed under reduced pressure. The crude was purified by column chromatography to afford (2-fluoro-4-nitrophenyl)methanamine (329 mg, 56 %).
  • Step 4 To a stirred solution of (2-fluoro-4-nitrophenyl)methanamine (131 mg, 0.77 mmol) in pyridine, cooled to 0 ° C, were added methanesulfonyl chloride (131 mg). The resulting reaction mixture was stirred for 1 h at room temperature. The mixture dissolved in
  • Step 5 To a stirred solution of N-(2-fluoro-4-nitrobenzyl)methanesulfonamide (187 mg, 0.75 mmol) in tetrahydrofuran and ethanol as co-solvent were added 10 % Pd / C (20 mg). The mixture was charged with hydrogen gas balloon. The resulting mixture was stirred for 15 h, then filtered using celite. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(4-amino-2-fluorobenzyl)methanesulfonamide (135 mg, 82 %) was obtained.
  • Step 6 To a stirred solution of N-(4-amino-2-fluorobenzyl)methanesulfonamide (135 mg, 0.618 mmol) in tetrahydrofuran and acetonitrile as co-solvent were added
  • Step 7 To a stirred solution of phenyl 3-fluoro-4-(methylsulfonamidomethyl)phenyl- carbamate (46 mg, 0.136 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3- yl)methanamine (37 mg, 0.136 mmol) in acetonitrile were added 4-dimethylaminopyridine (17 mg, 0.136 mmol). The reaction mixture was stirred for 15 h at 50 ° C. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo.
  • Exemplary compound 44 can be and exemplary compound 47was prepared in a similar manner.
  • Step 1 To a stirred solution of 2-(3-chloro-4-hydroxyphenyl)acetic acid (3 g, 16.078 mmol) in methanol (35 ml_) were added sulfuric acid (0.3 ml_). The reaction mixture was refluxed for 15 h and cooled to room temperature. The solvent was evaporated. The residue dissolved in ethyl acetate and extracted with NaHC0 3 . The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. Methyl 2-(3-chloro-4-hydroxyphenyl)acetate (3.557 g) was obtained as 99 % yield.
  • Step 2 To a stirred solution of methyl 2-(3-chloro-4-hydroxyphenyl)acetate (3.557 g, 17.73 mmol) and trimethylamine (2.5 ml_, 17.73 mmol) in dichloromethane. Triflic anhydride (3 ml_, 17.73 mmol) is added dropwise at 0 ° C. The reaction mixture was stirred for 2 h. The residue extracted in dichloromethane and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography to give methyl 2-(3-chloro-4-(trifluoromethylsulfonyloxy)- phenyl)acetate (5.15 g, 87 %).
  • Step 3 To a stirred solution of methyl 2-(3-chloro-4-(trifluoromethylsulfonyloxy)- phenyl)acetate (4.419 g, 13.283 mmol) in dimethylformamide were added zinc cyanide (1 .6 g, 13.681 mmol) and tetrakis(triphenylphosphine) palladium (1 .5 g, 1 .3283 mmol). The reaction mixture was stirred for 34 h at 80 ° C, then cooled to room temperature and diluted with ethyl acetate. The mixture was filtered using celite pad. The filtrate dissolved in ethyl acetate and extracted with NaHC0 3 . The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column
  • Step 4 To a stirred solution of methyl 2-(3-chloro-4-cyanophenyl)acetate (931 mg, 4.441 mmol) in dimethylformamide were added 60 % sodium hydride (178 mg, 4.441 mmol) and iodomethane (0.3 ml_, 4.441 mmol) at 0 ° C. The reaction mixture was stirred for 1 h at 0 ° C, then diluted with water. The residue dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography to give methyl 2-(3-chloro-4- cyanophenyl)propanoate (642 mg, 65 %).
  • Step 5 To a stirred solution of methyl 2-(3-chloro-4-cyanophenyl)propanoate (642 mg, 2.87 mmol) in co-solvent with tetrahydrofuran and water (1 :1 ) were added sodium hydroxide (287 mg, 7.175 mmol). The reaction mixture was stirred for 15 h at room temperature, then acidified to pH 3-4 with acetic acid. The residue dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Step 7 To a stirred solution of 2-(3-chloro-4-cyanophenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (158 mg, 0.361 mmol) in methanol, cooled to 0 ° C, were added di-ieri-butyl dicarbonate (158 mg, 0.722 mmol) and nickel(ll) chloride hexahydride (9 mg, 0.0361 mmol). Sodium borohydride (96 mg, 2.527 mmol) was added in small portions. The resulting reaction mixture was allowed to warm to room temperature and left to stir for 1 h.
  • Step 8 To a stirred solution of tert-butyl 2-chloro-4-(1 -oxo-1 -((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methylamino)propan-2-yl)benzylcarbamate (123 mg, 0.227 mmol) in dichloromethane (4 ml_), cooled to 0 ° C, was added trifluoroacetic acid (2 ml_). The resulting reaction mixture was stirred for 1 h at 0 ° C and 1 h at room temperature, then basified to pH 8-9 with aqueous NaHC0 3 . The mixture was filtered using celite pad.
  • Step 9 To a stirred solution of 2-(4-(aminomethyl)-3-chlorophenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (81 mg, 0.183 mmol) in pyridine, cooled to 0 ° C, was added methanesulfonyl chloride (81 mg). The resulting reaction mixture was stirred for 15 h at room temperature. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(3-Chloro-4-
  • Exemplary compounds 16, 56 and 62 were prepared or can be prepared in a similar manner.
  • Step 1 - 5 according to example 45.
  • Step 6 To a stirred solution of 2-(3-chloro-4-cyanophenyl)propanoic acid (224 mg, 1 .069 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (321 mg, 1 .175 mmol) in acetonitrile were added 1 -ethyl-3-(3-dimethylaminopropyl) carbodiimide (307 mg, 1 .064 mmol), 1 -hydroxybenzotriazole (217 mg, 1 .064 mmol) and triethylamine (0.4 ml, 2.673 mmol).
  • Step 7 To a stirred solution of 2-(3-chloro-4-cyanophenyl)-N-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (679 mg, 1 .460 mmol) in methanol, cooled to 0 ° C, were added di-terf-butyl dicarbonate (638 mg, 2.921 mmol) and NiCI 2 -6H 2 0 (35 mg, 0.147 mmol). Sodium borohydride (387 mg, 10.22 mmol) was then added in small portions. The reaction was exothermic and effervescent.
  • Step 8 To a stirred solution of tert-butyl 2-chloro-4-(1 -((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methylamino)-1 -oxopropan-2-yl)benzylcarbamate (390 mg, 0.685 mmol) in dichloromethane (4 ml_), cooled to 0 ° C were added trifluoroacetic acid (2 ml_). The resulting reaction mixture was stirred for 1 h at 0 ° C and 1 h at room temperature, then basified to pH 8-9 with aqueous sodium hydrogen carbonate. The mixture was filtered using celite pad.
  • Step 9 To a stirred solution of 2-(4-(aminomethyl)-3-chlorophenyl)-N-((2-(4-methylpiperidin- 1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (242 mg, 0.516 mmol) in pyridine, cooled to 0 ° C, were added methanesulfonyl chloride (242 mg). The resulting reaction mixture was stirred for 15 h at room temperature. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Exemplary compounds 25-29 and 58 were prepared or can be prepared in a similar manner.
  • Step 1 To a stirred solution of 1 -methoxy-2-nitrobenzene (3 g, 19.590 mmol) in
  • Step 2 To a stirred solution of ethyl 2-(3-methoxy-4-nitrophenyl)propanoate (683 mg, 2.697 mmol) in tetrahydrofuran and ethanol as co-solvent were added 10 % palladium on carbon (70 mg). The mixture was charged with H 2 (gas) balloon. The resulting mixture was stirred for 15 h, then filtered using celite. The filtrate removed in vacuo. The crude was purified by column chromatography. Ethyl 2-(4-amino-3-methoxyphenyl)propanoate (447 mg) was obtained as 74 % yield.
  • Step 3 To a stirred solution of ethyl 2-(4-amino-3-methoxyphenyl)propanoate (447 mg, 2.002 mmol) in acetonitrile and water were added p-TsOH-H 2 0 (1 .142 g, 6.006 mmol), sodium nitrite (276 mg, 4.004 mmol) and potassium iodide (831 mg, 5.005 mmol). The reaction mixture was stirred for 4 h at room temperature. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. Ethyl 2-(4-iodo-3-methoxyphenyl)propanoate (468 mg) was obtained as 70 % yield.
  • Step 4 To a stirred solution of ethyl 2-(4-iodo-3-methoxyphenyl)propanoate (626 mg, 1 .873 mmol) in dimethylformamide were added zinc cyanide (227 mg, 1 .929 mmol) and
  • Step 5 To a stirred solution of ethyl 2-(4-cyano-3-methoxyphenyl)propanoate (222 mg, 0.952 mmol) in co-solvent with tetrahydrofuran and water (1 :1 ) were added sodium hydroxide (95 mg, 2.38 mmol). The reaction mixture was stirred for 15 h at room temperature, then acidified to pH 3-4 with acetic acid. The residue dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(4-Cyano-3- methoxyphenyl)propanoic acid (188 mg) was obtained as 96 % yield.
  • Step 6 To a stirred solution of 2-(4-cyano-3-methoxyphenyl)propanoic acid (0.458 mmol) and (2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (0.5038 mmol) in acetonitrile were added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (0.687 mmol), 1 - hydroxybenzotriazole (0.687 mmol) and triethylamine (1 .145 mmol). The reaction mixture was stirred for 15 h at room temperature. The residue dissolved in ethyl acetate and washed with water and brine.
  • Step 7 To a stirred solution of 2-(4-cyano-3-methoxyphenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (0.473 mmol) in methanol, cooled to 0 ° C, were added di-tert-butyl dicarbonate (0.946 mmol) and NiCI 2 -6 H 2 0 (0.0473 mmol). Nsodium borohydride (3.31 1 mmol) was then added in small portions. The reaction was exothermic and effervescent. The resulting reaction mixture was allowed to warm to room temperature and left to stir for 1 h.
  • Step 8 To a stirred solution of tert-butyl 2-methoxy-4-(1 -oxo-1 -((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methylamino)propan-2-yl)benzylcarbamate (0.274 mmol) in dichloromethane (4 mL), cooled to 0 ° C, were added trifluoroacetic acid (1 mL). The resulting reaction mixture was stirred for 2 h at 0 ° C and 2 h at room temperature, then basified to pH 8-9 with aq. NaHC0 3 . The mixture was filtered using celite pad.
  • Step 9 To a stirred solution of 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(pyrrolidin-1 -yl)- 6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (147 mg, 0.337 mmol) in pyridine, cooled to 0 ° C, were added methanesulfonyl chloride (0.03 mL). The resulting reaction mixture was stirred for 20 min at room temperature. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Step 3 10% Palladium on carbon (one-tenth amount of the amide) is added to N-(2- methoxy-4-nitrobenzyl)methanesulfonamide in tetrahydrofuran and ethanol (1 :1 ) solvent. Hydrogen gas is charged and the reaction is stirred at room temperature for 15 h. Palladium is removed by celite pad filtration. After evaporate solvent, it is purified by column
  • Step 4 Phenyl chloroformate (1 .05 equiv.) is dropwised to N-(4-amino-2- methoxybenzyl)methanesulfonamide which is dissolved in tetrahydrofuran and acetonitril solution and pyridine (1 .2 equiv.) is added. The reaction is stirred at room temperature for 3 h and water is added. Organic layer is extracted with ethylacetate, washed with water and dried over magnesium sulfate . The mixture is purified by column chromatography
  • Step 5 Phenyl 3-methoxy-4-(methylsulfonamidomethyl)phenylcarbamate is dissolved in acetonitrile and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (1 equiv.), dimethylaminopyridine (1 equiv.) is added to the solution.
  • Step 1 To a stirred solution of 1 -methoxy-2-nitrobenzene (3 g, 19.59 mmol) in
  • Step 2 To a stirred solution of ethyl 2-(3-methoxy-4-nitrophenyl)propanoate (683 mg, 2.697 mmol) in tetrahydrofuran and ethanol as co-solvent were added 10 % Pd / C (70 mg). The mixture was charged with H 2 (gas) balloon. The resulting mixture was stirred for 15 h, then filtered using celite. The filtrate removed in vacuo. The crude was purified by column chromatography. Ethyl 2-(4-amino-3-methoxyphenyl)propanoate (447 mg) was obtained as 74 % yield.
  • Step 3 To a stirred solution of ethyl 2-(4-amino-3-methoxyphenyl)propanoate (447 mg, 2.002 mmol) in acetonitrile and water were added p-toluenesulfonic acid monohydrate (1 .142 g, 6.006 mmol), sodium nitrite (276 mg, 4.004 mmol) and potassium iodide (831 mg, 5.005 mmol). The reaction mixture was stirred for 4 h at room temperature. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. Ethyl 2-(4-iodo-3-methoxyphenyl)propanoate (468 mg) was obtained as 70 % yield.
  • Step 4 To a stirred solution of ethyl 2-(4-iodo-3-methoxyphenyl)propanoate (626 mg, 1 .873 mmol) in dimethylformamide were added zinc cyanide (227 mg, 1 .929 mmol) and
  • Step 5 To a stirred solution of ethyl 2-(4-cyano-3-methoxyphenyl)propanoate (222 mg, 0.952 mmol) in co-solvent with tetrahydrofuran and water (1 :1 ) were added sodium hydroxide (95 mg, 2.38 mmol). The reaction mixture was stirred for 15 h at room temperature, then acidified to pH 3-4 with acetic acid. The residue dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 2-(4-Cyano-3- methoxyphenyl)propanoic acid (188 mg) was obtained as 96 % yield.
  • Step 6 To a stirred solution of 2-(4-cyano-3-methoxyphenyl)propanoic acid (94 mg, 0.458 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (138 mg, 0.5038 mmol) in acetonitrile were added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (132 mg, 0.687 mmol), N-hydroxybenzotriazole (93 mg, 0.687 mmol) and triethylamine (0.16 ml_, 1 .145 mmol). The reaction mixture was stirred for 15 h at room temperature.
  • Step 7 To a stirred solution of 2-(4-cyano-3-methoxyphenyl)-N-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (218 mg, 0.473 mmol) in methanol, cooled to 0 ° C, were added di-ieri-butyl dicarbonate (206 mg, 0.946 mmol) and nickel(ll) chloride hexahydride (1 1 mg, 0.0473 mmol). Sodium borohydride (125 mg, 3.31 1 mmol) was added in small portions. The resulting reaction mixture was allowed to warm to room temperature and left to stir for 1 hour.
  • Step 8 To a stirred solution of tert-butyl 2-methoxy-4-(1 -((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methylamino)-1 -oxopropan-2-yl)benzylcarbamate (155 mg, 0.274 mmol) in dichloromethane (4 ml_), cooled to 0 ° C, was added trifluoroacetic acid (1 ml_). The resulting reaction mixture was stirred for 2 h at 0 ° C and 2 h at room temperature, then basified to pH 8-9 with NaHC0 3 . The mixture was filtered using celite pad.
  • Step 9 To a stirred solution of 2-(4-(aminomethyl)-3-methoxyphenyl)-N-((2-(4- methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (65 mg, 0.139 mmol) in pyridine, cooled to 0 ° C, was added methanesulfonyl chloride (65 mg). The resulting reaction mixture was stirred for 15 h at room temperature. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Step 1 To a stirred solution of added potassium tert. butoxide (2.05 g, 18.3 mmol ) in dimethylformamide (10 mL) were slowly added the mixture of 1 -methyl-2-nitrobenzene (1 g, 7.29 mmol ) and ethyl-2-chloropropionate(0.98 mL, 7.70 mmol) at -30°C. The reaction mixture was stirred for 10 min and warmed to room temperature. The residue was dissolved with ethyl acetate and neutralized with NaHC0 3 . The organic layer was washed with water two times, then dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. Ethyl 2-(3-methyl-4-nitrophenyl)propanoate (1 .2 g) was obtained as 70 % yield.
  • Step 2 Ethyl 2-(3-methyl-4-nitrophenyl)propanoate (1 .2 g, 5.05 mmol ) was dissolved in methanol and tetrahydrofuran(1 :1 , 15 mL). 10 % Pd / C (180 mg, 10 % ) was added to it. The resulting mixture was stirred at room temperature for 3 h under H 2 . TLC showed complete consumption of starting material. The mixture was filtered through celite bed and the filterate was concentrated under reduced pressure. The crude was purified by column
  • Step 3 To a stirred solution of ethyl 2-(4-amino-3-methylphenyl)propanoate (944 mg, 4.55 mmol) in acetonitrile, p-TsOH.H 2 0 (2.62 g, 13.66 mmol) was dropped slowly. The reaction mixture was activated for 10 min. Then NaN0 2 (629 mg, 9.1 1 mmol) in water was added dropwise. The mixture was stirred for 10 min. Then potassium iodide (1 .89 g, 1 1 .39 mmol) in water was added slowly dropwise. The reaction mixure was stirred at room temperature for 4 h.
  • Step 4 To a stirred solution of ethyl 2-(4-iodo-3-methylphenyl)propanoate (1 .22 g, 5.34 mmol) in anhydrous dimethylformamide were added zinc cyanide (645 mg, 5.50 mmol) and tetrakis(triphenylphosphine) palladium (617 mg, 0.53 mmol). The reaction mixture was refluxed for overnight then cooled to room temperature. The mixture was filtered using celite pad and the filtrate was evaporated. The residue was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to get the crude. The crude was purified by column chromatography. Ethyl 2-(4-cyano-3-methylphenyl)propanoate(1 .05 g) was obtained as 90 % yield.
  • Step 5 To a stirred solution of ethyl 2-(4-cyano-3-methylphenyl)propanoate (1 .05 g, 4.82 mmol) in co-solvent with tetrahydrofuran and water (1 :1 ) were added sodium hydroxide (482 mg, 12.06 mmol). The reaction mixture was stirred for overnight at room temperature, then acidified to pH 3-4 with acetic acid. The residue was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude 2-(4-cyano-3-methylphenyl)propanoic acid (1 .1 g) was obtained as 99 % yield.
  • Step 6 To a stirred solution of 2-(4-cyano-3-methylphenyl)propanoic acid (100 mg, 0.53 mmol) in acetonitrile were added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (152 mg, 0.80 mmol), 1 -hydroxybenzotriazole (107 mg, 0.80 mmol), (2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methanamine (143 mg, 0.58 mmol) and triethylamine (0.18 mL, 1 .33 mmol). The reaction mixture was stirred for overnight at room temperature.
  • Step 7 To a stirred solution of 2-(4-cyano-3-methylphenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (90 mg, 0.22 mmol) in ethanol was cooled to 0 ° C and added NiCI 2 -6H 2 0 (51 mg, 0.22 mmol) and stirred more than 15mins. Sodium borohydride (57 mg, 1 .51 mmol) was then added in small portions. The reaction was exothermic and effervescent. The resulting reaction mixture was allowed to warm to room temperature and left to stir for 2h. The mixture was filtered using celite pad. The filtrate was concentrated was evaporated.
  • Step 8 To a stirred solution of 2-(4-(aminomethyl)-3-methylphenyl)-N-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (109 mg, 0.26 mmol) in pyridine was added methanesulfonylchloride (0.03 mL, 0.42 mmol) The reaction mixture was stirred for overnight at room temperature. The mixture was diluted with ethyl acetate and washed with 1 N HCI and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography.
  • Step 1 To a stirred solution of 2-methyl-4-nitroaniline (500 mg, 3.286 mmol) in acetonitrile and water were added p-TsOH-H 2 0 (1 .875 g, 9.858 mmol), sodium nitrite (453 mg, 6.572 mmol) and potassium iodide (1 .363 g, 8.215 mmol). The reaction mixture was stirred for 4 h at room temperature. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. 1 -lodo-2-methyl-4- nitrobenzene (812 mg) was obtained as 94 % yield.
  • Step 2 To a stirred solution of 1 -iodo-2-methyl-4-nitrobenzene (812 mg, 3.087 mmol) in dimethylformamide were added zinc cyanide (544 mg, 4.630 mmol) and
  • Step 3 To a stirred solution of 2-methyl-4-nitrobenzonitrile (407 mg, 2.510 mmol) in tetrahydrofuran was added 2 M borane-methyl sulfide complex in tetrahydrofuran (2.1 ml_). The reaction mixture was stirred for 15 h at 70 ° C. The mixture was cooled to room temperature, then quenched by water. The mixture dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. (2-Methyl-4- nitrophenyl)methanamine (178 mg) was obtained as 43 % yield.
  • Step 4 To a stirred solution of (2-methyl-4-nitrophenyl)methanamine (178 mg, 1 .071 mmol) in pyridine, cooled to 0 ° C, were added methanesulfonyl chloride (0.16 ml_, 2.0349 mmol). The resulting reaction mixture was stirred for 2 h. The mixture dissolved in dichloromethane and washed with 1 N HCI. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(2- methyl-4-nitrobenzyl)methanesulfonamide (100 mg) was obtained as 38 % yield.
  • Step 5 To a stirred solution of N-(2-methyl-4-nitrobenzyl)methanesulfonamide (100 mg, 0.409 mmol) in tetrahydrofuran and ethanol as co-solvent were added 10 % palladium on carbon (40 mg). The mixture was charged with H 2 (gas) balloon. The resulting mixture was stirred for 24 h, then filtered using celite. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(4-amino-2-methylbenzyl)methanesulfonamide (61 mg) was obtained as 70 % yield.
  • Step 6 To a stirred solution of N-(4-amino-2-methylbenzyl)methanesulfonamide (61 mg, 0.285 mmol) in tetrahydrofuran and acetonitrile as co-solvent were added
  • Step 7 To a stirred solution of phenyl 3-methyl-4-
  • Step 2 1 -lodo-2-methyl-4-nitrobenzene, Pd 2 (dba) 3 , zinc cyanide were placed in round flask charged with N 2 and dissolved in dimethylformamide. The reaction mixture was stirred at 120 'C for 24 h and cooled to room temperature. Extracted with ethyl acetate and washed with 2N NH 4 OH solution. The organic layer was washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was purified on a silica gel column using ethylacetate- hexane as solvent system to give 2-methyl-4-nitrobenzonitrile.
  • Step 3 To the solution of 2-methyl-4-nitrobenzonitrile in tetrahydrofuran, 2 M borane-methyl sulfide complex in tetrahydrofuran was drop-wised slowly and the mixture refluxed during a day. After cooling the reaction to room temperature, water was drop-wised to removed left borane and extracted with ethyl acetate, washed with water several times. The crude resultant was purified by column chromatography and (2-methyl-4-nitrophenyl)methanamine was obtained.
  • Step 4 Pyridine was added to the solution of (2-methyl-4-nitrophenyl)methanamine in dichloromethane, followed by methanesulfonylchloride. The reaction mixture was stirred for 2 h at room temperature. The mixture was diluted with ethyl acetate and washed with 1 N HCI and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography. N-(2-methyl-4- nitrobenzyl)methanesulfonamide was obtained.
  • Step 5 10% Palladium on carbon was added to N-(2-methyl-4- nitrobenzyl)methanesulfonamide solution in methanol and the mixture was charged with H 2 . After stirring the reaction mixture for 15 h, the mixture was filtered using Celite and purified by column chromatography to get N-(4-amino-2-methylbenzyl)methanesulfonamide in hand.
  • Step 6 To a stirred solution of N-(4-amino-2-methylbenzyl)methanesulfonamide in acetone/tetrahydrofuran was added pyridine at 0 ° C. The reaction mixture was stirred for 3 h at room temperature. The residue was dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography and phenyl 3-methyl-4- (methylsulfonamidomethyl)phenylcarbamate was obtained.
  • Step 7 To a stirred solution of phenyl 3-methyl-4-(methylsulfonamidomethyl)- phenylcarbamate in acetonitrile was added (2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methanamine derivatives synthesized previously, followed by dimethylaminopyridine (1 equiv.). The reaction mixture was stirred for 15 h at 50 °C. The residue was dissolved in dichloromethane and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo.
  • Step 1 (4-Bromo-2-fluorophenyl)methanamine (924 mg, 4.53 mmol) was dissolved in pyridine and ethane sulfonyl chloride (0.82 mL, 8.60 mmol) was added to the solution at 0 °C. The mixture was stirred for 1 h at 0 °C. Then, the mixture was quenched with 1 N HCI and extracted with ethyl acetate.
  • Step 2 To a solution of N-(4-bromo-2-fluorobenzyl)ethanesulfonamide (305 mg, 1 .03 mmol) in dimethylformamide, Manganese (1 13 mg, 2.06 mmol), (2,2'-Bipyridine)nickel(ll)-dibromide (27 mg, 0.07 mmol), ethyl 2-chloropropanoate (0.17 mL, 1 .34 mmol) was added. It was followed by addition of trifluoroacetic acid (0.002 ml_, 0.028 mmol). The mixture was stirred for 24 h at 65 °C. The reaction mixture was quenched by concentrated HCI (7 drops).
  • Step 3 To a solution of ethyl 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoate (60 mg, 0.189 mmol) in tetrahydrofuran and water co-solvent, sodium hydroxide (19 mg) was added at room temperature. The mixture was stirred for overnight and extracted with ethyl acetate, dried over magnesium sulfate, the solvent was evaporated in vacuo. It was purified by column chromatography to give 2-(4-(ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid (55 mg).
  • Step 4 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid (60 mg, 0.207 mmol) and (2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (57 mg, 0.228 mmol) were dissolved in 1 ,4-dioxane.
  • Step 1 -3 according to example 54.
  • Step 4 2-(4-(Ethylsulfonamidomethyl)-3-fluorophenyl)propanoic acid (55 mg , 0.19 mmol) and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (57 mg, 0.209 mmol) was dissolved in 1 ,4-dioxane, followed by addition of 1 -hydroxybenzotriazole (39 mg , 0.285 mmol), 1 -ethyl-3-(3-dimethylaminopropyl) carbodiimide (55 mg , 0.285 mmol) and triethylamine (0.066 ml_ , 0.475 mmol).
  • Step 1 N-Bromosuccinimide (1 .51 g , 8.509 mmol) was added to a solution of 1 -methyls- nitrobenzene (1 .2 g, 7.735 mmol) in carbon tetrachloride. At room temperature 70% benzoyl peroxide (120 mg) was added to the mixture and refluxed for 24 h.
  • Step 2 To a solution of 1 -(bromomethyl)-4-nitrobenzene (1 .1 g , 4.69 mmol) in
  • Step 3 To a stirred solution of 2-(4-nitrobenzyl)isoindoline-1 ,3-dione (1 .6 g , 5.33 mmol) in tetrahydrofuran was added hydrazine monohydrate (4 equivalents). The mixture was stirred at reflux for 6 h, until complete consumption, as evidenced by TLC analysis, the mixture was cooled to room temperature. The mixture was treated with potassium bicarbonate to adjust the pH to 12-13. It was extracted with ethyl acetate, washed by brine, dried over magnesium sulfate and concentrated under reduced pressure.
  • Step 4 Chlorosulfonyl isocyanate (0.063 ml_) and tert-butanol (0.07 ml) was mixed in dichloromethane (5 ml_). After 10 minutes, a solution of (4-nitrophenyl)methanamine (100 mg, 0.657 mmol) in dichloromethane was added and stirred for 30 minutes at 50 ° C. The mixture was allowred to cool to room temperature, triethylamine (0.1 1 ml_) was added and the mixture was stirred for 3 h more. The reaction mixture was extracted with ethyl acetate, washed by brine and dried over magnesium sulfate.
  • Step 5 10% Pd / C (7 mg) was added to a solution of tert-butyl N-(4- nitrobenzyl)sulfamoylcarbamate (65 mg) in ethanol and tetrahydrofuran. The mixture was charged with hydrogen gas balloon and stirred for 6 h at room temperature. The mixture was filtered using celite and evaporated in vacuo to gave tert-butyl N-(4-aminobenzyl)sulfamoyl- carbamate (58 mg, 98 %).
  • Step 6 To a stirred solution of tert-butyl N-(4-aminobenzyl)sulfamoylcarbamate (86 mg , 0.285 mmol) in tetrahydrofuran - acetonitrile (1 :1 ) was added pyridine (0.03 ml_, 0.342 mmol) and phenylchloroformate (0.04 ml_, 0.3 mmol) at 0 ° C. The mixture was stirred at 0 ° C for 30 min and heated up to room temperature, then it was stirred for 30 min. The mixture was extracted with ethyl acetate, washed by brine, dried over magnesium sulfate and
  • Step 7 tert-Butyl N-(4-(3-((phenylcarbamate)methyl)ureido)benzyl)sulfamoylcarbamate (58 mg , 0.138 mmol) was dissolved in acetonitrile. (2-(Pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin- 3-yl)methanamine (38 mg, 0.138 mmol) and 4-dimethylaminopyridine (16 mg) were added to the solution. The reaction mixture was stirred for overnight at 50 °C. The mixture was extracted with ethyl acetate and washed with brine.
  • Step 8 To a solution of tert-butyl N-(4-(3-((2-(pyrrolidin-1 -yl)-6-(trifluoromethyl)pyridin-3- yl)methyl)ureido)benzyl)sulfamoylcarbamate (70 mg , 0.122 mmol) in dichloromethane (6 mL) trifluoroacetic acid (2ml_) was added at 0 °C. The mixture was stirred for 30 min at 0 °C and for 2 h at room temperature. The mixture was neutralized by sodium bicarbonate to pH 7-8, extracted with ethyl acetate and washed with brine.
  • Step 1 -6 according to example 57.
  • Step 7 tert-Butyl N-(4-(3-((phenylcarbamate)methyl)ureido)benzyl)sulfamoylcarbamate (58 mg , 0.138 mmol) was dissolved in acetonitrile, (2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methanamine (38 mg, 0.138 mmol) and 4-dimethylaminopyridine (16 mg) were added to the solution. The reaction mixture was stirred for overnight at 50 ° C. The mixture was extracted with ethyl acetate, washed by brine and dried over magnesium sulfate.
  • Step 8 To a solution of tert-butyl N-(4-(3-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate (88 mg , 0.147 mmol) in dichloromethane (6 mL) , tetrahydrofuran (2 mL) is added at 0 ° C. The mixture was stirred for 30 min at 0 °C and stirred for 2 h more at room temperature. After neutralisation by sodium bicarbonate to pH 7-8 the mixture was extracted with ethyl acetate and washed by brine.
  • Step 1 N-Bromosuccinimide (1 .27 g, 7. 09 mmol) was added to a solution of 2-fluoro-1 - methyl-4-nitrobenzene (1 .0 g, 6.446 mmol) in carbon tetrachloride. At room temperature 70% benzoyl peroxide (150 mg) was added to the mixture and refluxed for 24 h.
  • Step 2 To a solution of 1 -(bromomethyl)-2-fluoro-4-nitrobenzene (1 .05 g , 4.48 mmol) in dimethylformamide, potassium phthalimide (1 .8 g , 9.852 mmol) was added. The mixture was reacted for overnight, extracted with ethyl acetate and washed by brine (3 x 20 ml_).
  • Step 3 To a stirred solution of 2-(2-fluoro-4-nitrobenzyl)isoindoline-1 ,3-dione (1 .35 g , 4.48 mmol) in tetrahydrofuran was added hydrazine monohydrate (1 .3 ml_). The mixture was stirred at reflux for 6 h, until complete consumption, as evidenced by TLC analysis, the mixture was cooled to room temperature. The mixture was treated with potassium
  • Step 4 Chlorosulfonyl isocyanate (0.1 ml_) and tert-butanol (0.12 ml) was mixed in dichloromethane (5 ml_). After 10 minutes, a solution of (2-fluoro-4-nitrophenyl)methanamine (200 mg, 1 .176 mmol) in dichloromethane was added and stirred for 30 minutes at 50 ° C. The mixture was allowred to cool to room temperature, triethylamine (0.1 1 ml_) was added and the mixture was stirred for 3 h more. The reaction mixture was extracted with ethyl acetate, washed by brine and dried over magnesium sulfate.
  • Step 5 10% Pd / C (42 mg) was added to a solution of tert-butyl N-(2-fluoro-4- nitrobenzyl)sulfamoylcarbamate (135 mg) in ethanol and tetrahydrofuran. The mixture was charged with hydrogen gas balloon and stirred for 6 h at room temperature. The mixture was filtered using celite and evaporated in vacuo to tert-butyl N-(4-amino-2- fluorobenzyl)sulfamoylcarbamate (127 mg, 99 %).
  • Step 6 To a stirred solution of tert-butyl N-(4-amino-2-fluorobenzyl)sulfamoylcarbamate (127 mg , 0.398 mmol) in tetrahydrofuran - acetonitrile (1 :1 ) was added pyridine (0.04 ml_ , 0.478 mmol) and phenylchloroformate (0.05 ml_, 0.418 mmol) at 0 ° C. The mixture was stirred at 0 ° C for 30 min and heated up to room temperature, then it was stirred for 30 min.
  • Step 7 Tert-butyl N-(2-fluoro-4-(phenylcarbamate)methyl)ureido)benzyl)sulfamoylcarbamate (60 mg, 0.137 mmol) was dissolved in acetonitrile. (2-(Pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methanamine (37 mg, 0.137 mmol) and 4-dimethylaminopyridine (17 mg) were added to the solution. The reaction mixture was stirred for overnight at 50 °C. The mixture was extracted with ethyl acetate and washed with brine.
  • Step 8 To a solution of tert-butyl N-(2-fluoro-4-(3-((2-(pyrrolidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate (60 mg , 0.102 mmol) in dichloromethane (6 ml_) was added trifluoroacetic acid (2 ml_) at 0 °C. The mixture was stirred for 30 min at 0 °C and for 2 h at room temperature. The mixture was neutralized by sodium bicarbonate to pH 7-8, extracted with ethyl acetate and washed with brine.
  • Step 1 -6 according to example 60.
  • Step 7 Tert-butyl N-(2-fluoro-4-(phenylcarbamate)methyl)ureido)benzyl)sulfamoyl carbamate (60 mg , 0.137 mmol) was dissolved in acetonitrile, (2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methanamine (37 mg, 0.137 mmol) and 4-dimethylaminopyridine (17 mg) were added to the solution. The reaction mixture was stirred for overnight at 50 ° C. The mixture was extracted with ethyl acetate, washed by brine and dried over magnesium sulfate.
  • Step 8 To a solution of tert-butyl N-(2-fluoro-4-(3-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)ureido)benzyl)sulfamoylcarbamate (60 mg , 0.097 mmol) in dichloromethane (6 ml_) , tetrahydrofuran (2 ml_) is added at 0 ° C. The mixture was stirred for 30 min at 0 °C and stirred for 2 h more at room temperature. After neutralisation by sodium bicarbonate to pH 7-8 the mixture was extracted with ethyl acetate and washed by brine.
  • Step 1 (4-Bromo-2-fluorophenyl)methanamineis stirred in pyridine and methanesulfonyl chloride (1 .9 equiv.) is drop-wise at 0 'C. After remove in ice bath, reaction mixture is stirred at room-temperature during 1 h. The reaction is quenched with 1 N HCI and extracted with ethyl acetate. Extracted organic layer is dried over by magnesium sulfate. Reaction mixture is purified by column chromatography and obtained N-(4-bromo-2- fluorobenzyl)methanesulfonamide.
  • Step 2 N-(4-bromo-2-fluorobenzyl)methanesulfonamide is dissolved in anhydrous dimethylformamide and charged with N 2 .
  • Ethyl-2-chloro propionate (1 .3 equiv.) is dropped to the reactant and manganese (2 equiv.), nickel-2,2'-bipyridine (0.1 equiv.) is added with trifluoroacetic acid (0.026 equiv.).
  • the reaction is refluxed overnight.
  • the reaction mixture is warmed to ambient temperature.
  • the reaction is quenched with 1 N HCI and organic layer is extracted with diethyl ether.
  • the extracted organic layer is dried over magnesium sulfate, and concentrated into ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate that is carried onto the next step without purification.
  • Step 3 Crude ethyl 2-(3-fluoro-4-(methylsulfonamidomethyl)phenyl)propanoate is stirred in acetone at 0 'C, add K 2 C0 3 (1 .5 equiv.). After that, methyliodide (3 equiv.) is drop-wised and the reaction mixture is refluxed. After 15 h, the reaction mixture is quenched with water and extracted with ethyl acetate. The organic layer is dried over magnesium sulfate and concentrated. Reaction mixture was purified by column chromatography and obtained ethyl
  • Step 4 A solution of ethyl 2-(3-fluoro-4-((N-methylmethylsulfonamido)methyl)
  • Step 5 A solution of 2-(3-fluoro-4-((N-methylmethylsulfonamido)methyl)phenyl) propanoic acid in 1 ,4-dioxane was added N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (1 .5 equiv), 1 -hydroxybenzotriazole (1 .5 equiv), and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-
  • Step 0 (Intermediate A): One equiv. of chlorosulfonyl isocyanate is added drop-wise to a cold solution of tert-butyl alcohol (1 equiv.) in anhydrous dichloromethane. Then
  • Step 1 Sulfuric acid (0.3 mL) was added to a solution of 2-(3-fluoro-4-nitro-phenyl)-propionic acid in ethanol. The mixture was refluxed. After 6 h, the mixture was basified by aqueous sodium bicarbonate and extracted with ethyl acetate (ethyl acetate ). Drying over magnesium sulfate and evaporation of the ethyl acetate and purified by column chromatography (ethyl acetate : hexane) gave the ethyl 2-(3-fluoro-4-nitrophenyl)propanoate in pure form
  • Step 2 10 % Palladium on carbon was added to a solution ethyl 2-(3-fluoro-4- nitrophenyl)propanoate in ethanol and tetrahydrofuran and the mixture was charged with H 2 (g). After stirring the reaction mixture for 6 h, the mixture was filtered using celite and purified by column chromatography give ethyl 2-(4-amino-3-fluorophenyl)propanoate.
  • Step 3 A solution of p-TsOH H 2 0 (3 equiv.) in acetonitrile was added to a solution of ethyl 2- (4-amino-3-fluorophenyl)propanoate (1 equiv) in acetonitrile.
  • the resulting suspension of amine salt was cooled to 10-15 °C and to this was added, gradually, a solution of NaN0 2 (2 equiv.) and potassoim iodide (2.5 equiv.) in water.
  • the reaction mixture was stirred for 10 min then allowed to come to 20 °C and stirred until the starting material was consumed.
  • Step 4 Ethyl 2-(3-fluoro-4-iodophenyl)propanoate, Pd 2 (dba) 3 , dppf, cine powder and cine cyanide were placed in round flask charged with N 2 and DMA ( 0.02 equiv.) was dropped by syringe. The reaction mixture was stirred at 120'C for 15 h and cooled to room temperature. Extracted with ethyl acetate and washed with 2N NH 4 OH solution. The organic layer was washed with water, dried over sodium sulfate and concentrated in vacuo. The residue was purified on a silica gel column using ethyl acetate -hexane as solvent system to give ethyl 2- (4-cyano-3-fluorophenyl)propanoate.
  • Step 6 N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (1 .5 equiv), 1 -hydroxybenzotriazole (1 .5 equiv), and (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (1 equiv) are added to a solution of the 2-(4-cyano-3-fluorophenyl)propanoic aciddrop-wise triethylamine (2.5 equiv). The reaction mixture is stirred overnight at room temperature. The reaction is quenched with water and extracted with ethyl acetate. The extracted organic layer is dried over magnesium sulfate. After evaporate solvent, purified by column
  • Step 7 Nickel(ll) chloride hexahydride (1 equiv.) and 2-(4-cyano-3-fluorophenyl)-N-((2-(4- methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide are stirred in anhydrous ethanol during 15 min for activation. Sodium borohydride (7 equiv.) is added on it and react for 2 h. Adding celite to the reaction and filter it using celite packed filter, washing with ethanol.
  • reaction mixture is purified after concentration to give 2-(4-(aminomethyl)- 3-fluorophenyl)-N-((2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3- yl)methyl)propanamide.
  • Step 8 2-(4-(Aminomethyl)-3-fluorophenyl)-N-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide and intermediate (A) are dissolved in dichloromethane, drop-wise triethylamine ( 0.1 equiv.). The reaction is stirred for 15 h at room temperature and quenched with water. The organic layer is extracted by
  • Step 9 Trifluoroacetic acid (12 mL) is added to tert-butyl N-(2-fluoro-4-(1 -((2-(4- methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methylamino)-1 -oxopropan-2- yl)benzyl)sulfamoylcarbamate solutions in dichloromethane and the reaction is stirred for 4h at room temperature. Water is dropped to the mixture and organic compound is extracted with dichloromethane.
  • Step 1 To a stirred solution of (4-bromo-2-fluorophenyl)methanamine in pyridine was added methane sulfonylchloride. The reaction mixture was stirred for overnight at room
  • Step 2 N-(4-bromo-2-fluorobenzyl)methanesulfonamide, Pd 2 (dba) 3, dppf, cine powder and cine cyanide were placed in round flask charged with N 2 and DMA ( 0.02 equiv.) was dropped by syringe. The reaction mixture was stirred at 120 'C in sealed tube for 15 h. The reaction was cooled down until room temperature and extracted with ethyl acetate and washed with 2N NH 4 OH solution. The organic layer was washed with water, dried and concentrated in vacuo. The residue was purified on a silica gel column using ethyl acetate - hexane as solvent system to give N-(4-cyano-2-fluorobenzyl)methanesulfonamide.
  • Step 3 10% Palladium on carbon was added to N-(4-cyano-2- fluorobenzyl)methanesulfonamide solution in methanol and the mixture was charged with H 2 (g). After stirring the reaction mixture for 15 h, the mixture was filtered using Celite and purified by column chromatography to give N-(4-(aminomethyl)-2- fluorobenzyl)methanesulfonamide.
  • Step 4 To a stirred solution of N-(4-(aminomethyl)-2-fluorobenzyl)methanesulfonamide in acetone/tetrahydrofuran was added pyridine at 0 ° C. The reaction mixture was stirred for 3 h at room temperature. The residue was dissolved in ethyl acetate and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo. The crude was purified by column chromatography and phenyl 3-fluoro-4- (methylsulfonamidomethyl)benzylcarbamate was obtained.
  • Step 5 To a stirred solution of phenyl 3-fluoro-4-(methylsulfonamidomethyl)benzylcarbamate in acetonitrile was added (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3- yl)methanamine, followed by dimethylaminopyridine (1 equiv.). The reaction mixture was stirred for 15 h at 50 °C. The residue was dissolved in dichloromethane and washed with water and brine. The organic layer was dried over magnesium sulfate and filtered. The filtrate removed in vacuo.
  • Step 1 To the solution 2-(4-fluorophenyl)acetic acid (700 mg, 43.4 mmol ) in methanol was slowly added sulfuric acid (0.42 ml_,4.34 mmol, 0.1 eq) at room temperature. The reaction mixture was refluxed for 3 h at 70 °C under N 2. TLC showed complete consumption of starting material. The reaction mixture was cooled to room temperature. Solvent was removed in vacuo and extracted with ethyl acetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column chromatography to methyl 2- (4-fluorophenyl)acetate (660 mg, 84 %).
  • Step 2 To the cooled solution of sodium hydride (501 mg, 2.285 mmol, 60 % suspension in oil) in anhydrous tetrahydrofuran was added solution of methyl 2-(4-fluorophenyl)acetate (990 mg, 2.285 mmol) dropwise at 0 °C. Reaction mixture was stirred at room temperature for 1 h.TLC showed complete consumption of starting material. The reaction mixture was quenched with brine and extracted with ethyl acetate. The organic part was washed with brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to afford crude product which was purified by column chromatography to methyl 2- (4-fluorophenyl)propanoate (551 mg, 52 %)
  • Step 3 To a solution of methyl 2-(4-fluorophenyl)propanoate (200 mg, 19.5 mmol) in 14 mL of sulfuric acid at 0 °C was added 69 % HN0 3 (0.4 mL) dropwise over 5 min. After stirring for 35 min at 0 °C, the solution was diluted with ethyl acetate at 0 °C, and then the resultant solution was poured into cold water. Water layer was extracted with ethyl acetate. The combined organic layer was washed with water, brine then dried over sodium sulfate. After removing solvent in vacuo, the residue was purified by silica gel column chromatography to give methyl 2-(4-fluoro-3-nitrophenyl)propanoate (175 mg, 79 %)
  • Step 4 Starting material methyl 2-(4-fluoro-3-nitrophenyl)propanoate (1 .55 g, 1 .23 mmol) was dissolved in methanol. 20 % w/w Pd / C (10 wt %) was added to it. The resulting mixture was stirred at room temperature for 2 h under H 2 gas. TLC showed complete consumption of starting material. The mixture was filtered by celite bed and then the filterate was
  • Step 6 A mixture of methyl 2-(4-fluoro-3-iodophenyl)propanoate (530 mg, 1 .72 mmol), cuprous cyanide (309 mg, 3.45 mmol) and dimethylformamide (5 mL) was heated at 140 °C for 7 h. After the reaction was completed the mixture was cooled to room temperature, poured into water (100 mL), and stirred at room temperature for 0.5 h. and extracted with ethyl acetate (3 x 50 mL).
  • Step 7 A solution of methyl 2-(3-cyano-4-fluorophenyl)propanoate (250 mg, 1 .2 mmol) in water and tetrahydrofuran (1 :2, 30 mL) was treated with lithium hydroxide (3.0 mmol) at 0 °C and stirred for 2 h at room temperature. The mixture was diluted with water and
  • Step 8 A solution of 2-(3-cyano-4-fluorophenyl)propanoic acid (50 mg, 0.256 mmol) in 1 ,4 Dioxane was cooled in an ice bath and N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide (73 mg, 0.384 mmol), 1 -hydroxybenzotriazole (51 mg, 0.384 mmol), Triethylamine (72 ⁇ , 0.760 mmol) and the (2-(4-methylpiperidin-1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methanamine (70 mg, 0.256 mmol), were added consecutively. The reaction mixture was stirred overnight at room temperature. Water was added to the reaction mixture and extracted with
  • Step 9 To a stirred solution of 2-(3-cyano-4-fluorophenyl)-N-((2-(4-methylpiperidin-1 -yl)-6- (trifluoromethyl)pyridin-3-yl)methyl)propanamide (70 mg, 0.156 mmol) in dry ethanol (15 mL), cooled to 0°C, were added NiCI 2 -6 H 2 0 (37 mg, 0.156 mmol). Sodium borohydride (36 mg, 0.936 mmol) was then added in small portions over 10 min. The reaction was exothermic and effervescent.
  • Step 10 A cooled solution of 2 2-(3-(aminomethyl)-4-fluorophenyl)-N-((2-(4-methylpiperidin- 1 -yl)-6-(trifluoromethyl)pyridin-3-yl)methyl)propanamide (34 mg, 0.075 mmol) in
  • Exemplary compounds 67 and 68 can be prepared in a similar manner as example 64.
  • Exemplary compounds 69-72 can be obtained by chiral resolution of examples 67 and 68.
  • resolutions can be e.g. performed by chiral high performance liquid chromatography (HPLC) on a Chiralpak AD-H, 5 ⁇ , 250 x 20 mm. Products can be detected by a JASCO UV-1575 wavelength UV monitor.
  • HPLC high performance liquid chromatography
  • mobile phase can be used a mixture of n-hexane / ethanol (7:3, v/v) with a flow rate 19 mL/min at 25 °C.
  • the agonistic or antagonistic effect of the substances to be tested on the rat-species vanilloid receptor 1 can be determined using the following assay.
  • the influx of Ca 2+ through the receptor channel is quantified with the aid of a Ca 2+ -sensitive dye (type Fluo-4, Molecular Probes Europe BV, Leiden, the Netherlands) in a fluorescent imaging plate reader (FLIPR, Molecular Devices, Sunnyvale, USA).
  • a Ca 2+ -sensitive dye type Fluo-4, Molecular Probes Europe BV, Leiden, the Netherlands
  • FLIPR fluorescent imaging plate reader
  • Complete medium 50 ml_ HAMS F12 nutrient mixture (Gibco Invitrogen GmbH, Düsseldorf, Germany) with 10 % by volume of FCS (foetal calf serum, Gibco Invitrogen GmbH, Düsseldorf, Germany, heat-inactivated); 2mM L-glutamine (Sigma, Kunststoff, Germany); 1 % by weight of AA solution (antibiotic/antimyotic solution, PAA, Pasching, Austria) and 25 ng/mL NGF medium (2.5 S, Gibco Invitrogen GmbH, Düsseldorf, Germany)
  • Cell culture plate Poly-D-lysine-coated, black 96-well plates having a clear base (96-well black/clear plate, BD Biosciences, Heidelberg, Germany) are additionally coated with laminin (Gibco Invitrogen GmbH, Düsseldorf, Germany), the laminin being diluted with PBS (Ca-Mg- free PBS, Gibco Invitrogen GmbH, Düsseldorf, Germany) to a concentration of 100 ⁇ g/mL. Aliquots having a laminin concentration of 100 ⁇ g mL are removed and stored at -20 °C.
  • the aliquots are diluted with PBS in a ratio of 1 : 10 to 10 ⁇ g mL of laminin and respectively 50 ⁇ - of the solution are pipetted into a recess in the cell culture plate.
  • the cell culture plates are incubated for at least two hours at 37 °C, the excess solution is removed by suction and the recesses are each washed twice with PBS.
  • the coated cell culture plates are stored with excess PBS which is not removed until just before the feeding of the cells.
  • the vertebral column is removed from decapitated rats and placed immediately into cold HBSS buffer (Hank's buffered saline solution, Gibco Invitrogen GmbH, Düsseldorf, Germany), i.e. buffer located in an ice bath, mixed with 1 % by volume (per cent by volume) of an AA solution (antibiotic/antimyotic solution, PAA, Pasching, Austria).
  • HBSS buffer Horco Invitrogen GmbH, Düsseldorf, Germany
  • AA solution antibiotic/antimyotic solution
  • PAA antibiotic/antimyotic solution
  • PAA dorsal root ganglia
  • the DRG from which all blood remnants and spinal nerves have been removed, are transferred in each case to 500 ⁇ _ of cold type 2 collagenase (PAA, Pasching, Austria) and incubated for 35 minutes at 37 °C. After the addition of 2.5 % by volume of trypsin (PAA, Pasching, Austria), incubation is continued for 10 minutes at 37 °C. After complete incubation, the enzyme solution is carefully pipetted off and 500 ⁇ _ of complete medium are added to each of the remaining DRG.
  • the DRG are respectively suspended several times, drawn through cannulae No. 1 , No. 12 and No. 1 6 using a syringe and transferred to a 50 ml_ Falcon tube which is filled up to 15 ml_ with complete medium.
  • each Falcon tube is respectively filtered through a 70 ⁇ Falcon filter element and centrifuged for 1 0 minutes at 1 ,200 rpm and room temperature. The resulting pellet is respectively taken up in 250 ⁇ _ of complete medium and the cell count is determined.
  • the number of cells in the suspension is set to 3 x 1 0 5 per ml_ and 1 50 ⁇ _ of this suspension are in each case introduced into a recess in the cell culture plates coated as described hereinbefore. In the incubator the plates are left for two to three days at 37 °C, 5 % by volume of C0 2 and 95 % relative humidity.
  • the cells are loaded with 2 ⁇ of Fluo-4 and 0.01 % by volume of Pluronic F1 27 (Molecular Probes Europe BV, Leiden, the Netherlands) in HBSS buffer (Hank's buffered saline solution, Gibco Invitrogen GmbH, Düsseldorf, Germany) for 30 min at 37 °C, washed 3 times with HBSS buffer and after further incubation for 1 5 minutes at room temperature used for Ca 2+ measurement in a FLIPR assay.
  • the FLIPR protocol consists of 2 substance additions. First the compounds to be tested (10 ⁇ ) are pipetted onto the cells and the Ca 2+ influx is compared with the control (capsaicin 1 0 ⁇ ). This provides the result in % activation based on the Ca 2+ signal after the addition of 1 0 ⁇ of capsaicin (CP). After 5 minutes' incubation, 100 nM of capsaicin are applied and the Ca 2+ influx is also determined.
  • the compounds according to the invention display outstanding affinity to the VR1 /TRPV1 receptor (Table 2).
  • the value after thetician@"symbol indicates the concentration at which the inhibition (as a percentage) was respectively determined.

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EP12762601.8A 2011-09-26 2012-09-25 Aminsubstituierte methansulfonamidderivate als vanilloidrezeptorliganden Withdrawn EP2760836A1 (de)

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CN103917523A (zh) 2014-07-09
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MX2014003386A (es) 2014-06-23
CA2849350A1 (en) 2013-04-04
AR088003A1 (es) 2014-04-30
TW201326125A (zh) 2013-07-01
BR112014006927A2 (pt) 2017-04-04
WO2013045451A1 (en) 2013-04-04
JP2014530198A (ja) 2014-11-17
US20130079320A1 (en) 2013-03-28
AU2012314508A1 (en) 2014-02-27

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